VNOTES and Vaginal Hysterectomy for Benign Indications
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age40-80
SponsorDr. Lutfi Kirdar Kartal Training and Research Hospital
About this trial
This study aimed to compare the surgical outcomes of Vaginal Natural Orifice Transluminal Endoscopic Surgery (vNOTES) and conventional vaginal hysterectomy (VH) for benign gynecological conditions.
A prospective analysis will conducted at a tertiary hospital from January 2025 to February 2025. Patients aged 40-80 who underwent hysterectomy for benign indications will included. Outcomes will assessed included surgical outcomes, Visual Analog Scale (VAS) pain scores, and complication rates.
Eligibility criteria
Qualifiers
aged between 40 and 80 years
undergo hysterectomy for benign gynecological conditions
Disqualifiers
history of urogynecological surgery (including pelvic organ prolapse surgery and mid-urethral sling procedures),
suspected gynecologic malignancies,
endometriosis,
tubal-ovarian abscesses,
Trial design
Treatments tested in this trial
- vNOTES
- vaginal hysterectomy
Treatment groups
100 Participants
are divided into 2 treatment groupsLocations
1Kartal Dr Lütfi Kirdar City Hospital34865, Istanbul Turkey (Türkiye)
Sponsors and collaborators
Dr. Lutfi Kirdar Kartal Training and Research Hospital
Lead sponsor
Source ClinicalTrials.gov