Progression

10

Review clinical trials related to Progression. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Construction of a Cohort of Elderly Patients With Atrial Fibrillation in Rural China

Atrial fibrillation (AF) is a common arrhythmia in aging populations and is strongly associated with an increased risk of heart failure (HF) and adverse cardiovascular outcomes. However, early detection of HF among patients with AF remain inadequate in rural settings. This study aims to screen for HF among older adults with AF in rural China and to conduct long-term follow-up in order to observe the disease progression in patients with AF. This study will recruit at least 2,500 elderly individuals aged between 65 and 80 years, with confirmed diagnoses of AF, residing in rural areas. Participants will undergo HF screening using NT-proBNP testing and echocardiographic assessment. Additionally, data will be collected on electrocardiographic signals, seismocardiography, voice, and demographic characteristics. Following data collection, participants will be followed up every three months to monitor the incidence and progression of HF as well as the occurrence of adverse cardiovascular events.

Participants needed: 2,500
Trial details
Age: 65-80Biological sex: AllType: ObservationalSponsor: Jiangsu Taizhou People's HospitalUpdated: May 28, 2026Locations: 1
Eligibility criteria

Permanent residents with local household registration in rural China. [+4]

Expected life expectancy of less than 3 months. [+5]

Status: Recruiting

Trial Of Stereotactic Body Radiation Therapy (SBRT) for Oligoprogression on Immune Checkpoint Inhibitors (ICI) in Metastatic Renal Cell Carcinoma

This Phase II trial will evaluate progression-free survival after Stereotactic Body Radiation Therapy to oligoprogressive (1-5) lesions in metastatic renal cell carcinoma patients on any immune checkpoint inhibitor-containing regimen with last dose of systemic therapy within 3 months prior to trial enrollment.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Yale UniversityUpdated: Dec 4, 2025Locations: 1
Eligibility criteria

Be willing and able to provide written informed consent/assent for the trial [+13]

Has had radiation therapy within 2 weeks of the first protocol treatment. [+12]

Status: Recruiting

Liver Disease and Other Systemic Diseases

Examine the association of chronic liver diseases (including hepatitis B, hepatitis C, alcoholic liver disease, fatty liver, liver cirrhosis, and hepatocellular carcinoma) with other systemic diseases by retrospectively analyzing the data from the Hospital Database of Buddhist Tzu Chi Medical Foundation.

Participants needed: 15,000
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical FoundationUpdated: Sep 19, 2025Locations: 1
Eligibility criteria

Individuals who visited the gastroenterology clinics of the Tzu Chi Hospitals, B...

Age younger than 18 or older than 99 years

Status: Recruiting

Omitting CTV for Primary Tumor in LS-SCLC

This randomized controlled non-inferior trial prospectively enrolled patients with limited-stage small cell lung cancer (LS-SCLC). Patients in the experimental group would receive radiotherapy with omission of the clinical target volume (CTV) for the primary tumor, while those in the control group would receive radiotherapy including CTV. The efficacy and toxicity of the two groups are compared to provide evidence for the radiotherapy of LS-SCLC. The target volume of LS-SCLC may be reduced by omitting CTV without increasing local recurrence but potentially reducing the dose to organs at risk and the side effects.

Participants needed: 852
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: Sun Yat-sen UniversityUpdated: Jun 6, 2025Locations: 2
Eligibility criteria

Small cell lung cancer confirmed by histology or cytology; TNM stage IA-IIIC (AJ... [+8]

Other malignant tumors (prior or concurrent), except those that have been curati... [+7]

Status: Recruiting

The Norwegian World Health Organisation Labour Care Guide Trial (NORWEL)

Appropriate and timely care during birth is critical to the survival and health of women and their babies. In 2020, the World Health Organization (WHO) presented the Labour Care Guide (LCG) as the new recommended tool for monitoring birth and assessing progression, replacing the WHO partograph. This evidence-based guide was designed to ensure improved quality and safety of care, and to avoid unnecessary interventions during birth. The LCG was developed to be used in all settings globally, but it has only been tested in health facilities in South America, Asia and Africa, while it has not been tested in high-income settings. Implementing a new guideline for monitoring birth is a comprehensive operation that will affect both the national economy, health systems, and individual patients; therefore, further research on the possible advantages is needed before national enrolment. Hence, the trial proposed in this application is crucial to form the required foundation of knowledge. The trial will be conducted in labour wards at ten hospitals, covering all health regions in Norway, and the established Norwegian Research Network for Clinical Studies in Obstetrics (NORBIRTH), with dedicated local principal investigators, will provide a robust research environment. This trial will test the effect of the LCG. Results from this trial will provide knowledge needed to determine a future implementation of the LCG in Norway.

Participants needed: 23,650
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Ostfold Hospital TrustUpdated: Apr 4, 2025Locations: 10
Eligibility criteria

Women in active labour [+1]

None

Status: Recruiting

Everolimus 5 mg vs 10 mg/Daily for Patients With Neuroendocrine Tumors

Everolimus is approved in many countries to treat patients with advanced/metastatic well-differentiated neuroendocrine tumors (NET), providing median progression-free survival times of approximately 12 months across different types of NET. However, it is can cause severe adverse effects. Phase I trial demonstrated that a dose of 5mg/day/week was sufficient to inhibit cell proliferation by blocking the mTOR pathway. This is a randomized, open-label, phase II near-equivalence clinical trial of oral everolimus 5 mg vs 10 mg oral/daily and continuously in patients with Grade 1 or Grade 2 metastatic NET, with tumor progression or intolerance to at least one line of treatment and with radiological disease progression within 6 months.

Participants needed: 100
Trial details
Phase: Phase 2Age: 16+Biological sex: AllType: InterventionalSponsor: AC Camargo Cancer CenterUpdated: Jun 25, 2024Locations: 2
Eligibility criteria

Histological confirmation of well-differentiated Grade 1/Grade 2 NET from gastro... [+8]

Aggressive disease requiring cytotoxic therapy [+2]

Status: Not yet recruiting

Tumor Cell Plasticity and Aggressiveness in Human Non-small Cell Lung Cancer

Tumor cell plasticity (TCP) is a conubium of processes which lead to re-activation of developmental programs correlating with epithelial-to-mesenchymal transition, and ultimately leading to acquisition of stem cell properties and transdifferentiation potential. Little is known about the molecular mechanisms governing TCP in lung adenocarcinoma (LUAD), i.e. the most frequent lung cancer subtype. The investigators recently identified prognostic 7-miRNAs/10-mRNAs signatures which accurately identified aggressive LUAD among patients with early-stage disease (Stage I). Furthermore, the investigators showed that such tumors show TCP features i.e. mesenchymal and stem-cell traits, high-metastatic potential. Here, the investigators aim to explore by RNAseq and by immunophenotyping at a single-cell level (scRNAseq/AbSeq), the molecular features of aggressive LUAD to unveil the mechanisms triggering TCP. The investigators predict thier results will be relevant for the development of more effective therapeutic protocols for management of aggressive LUAD.

Participants needed: 20
Trial details
Biological sex: AllType: ObservationalSponsor: Casa Sollievo della Sofferenza IRCCSUpdated: Jun 18, 2024
Eligibility criteria

patients diagnosed with lung adenocarcinoma [+2]

patients with a previous history of cancer [+1]

Status: Not yet recruiting

A Single-center Study on the Effect of Systemic/Selective Lymph Node Dissection on the Prognosis of Ground Glass Nodules Smaller Than 3cm and With Components With Consolidation/Tumor Ratio Between 0.5-1

A single-center study on the effect of systemic/selective lymph node dissection on the prognosis of ground glass nodules smaller than 3cm and with components with consolidation/tumor ratio between 0.5-1

Participants needed: 500
Trial details
Age: 25-75Biological sex: AllType: InterventionalSponsor: Shanghai Zhongshan HospitalUpdated: Jan 11, 2022
Eligibility criteria

1.Aged between 25 and 75 years; [+5]

1. Patients with a history of lung surgery; [+6]

Status: Recruiting

A Prospective, Two-center, Single Arm Phase II Clinical Study to Evaluate Safety and Effectiveness of Ablation Therapy in the Treatment of Lung Cancer Presenting as Ground-glass Nodules

A prospective, two-center, single arm phase II clinical study to evaluate safety and effectiveness of ablation therapy in the treatment of lung cancer presenting as ground-glass nodules

Participants needed: 120
Trial details
Phase: Phase 2Age: 18-85Biological sex: AllType: InterventionalSponsor: Shanghai Zhongshan HospitalUpdated: May 27, 2021Locations: 1
Eligibility criteria

Aged between 18 and 85 years; [+5]

Patients who participated in any drug and / or medical device clinical trials wi... [+5]

Status: Recruiting

A Multiple-center Study on the Effect of Different Ways of Lymph Node Dissection on the Prognosis of Ground Glass Nodules Smaller Than 3cm and With More Than 50% Solid Components

A multiple-center study on the effect of different ways of lymph node dissection on the prognosis of less than 3cm ground glass nodules with more than solid components

Participants needed: 1,500
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Shanghai Zhongshan HospitalUpdated: Oct 9, 2020Locations: 1
Eligibility criteria

Aged between 18 and 75 years; [+5]

Patients with a history of using immunosuppressive or hormonal drugs; [+3]