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Starting soon Not applicable

VNOTES and Vaginal Hysterectomy for Benign Indications

NCT06776718 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-01
Last updated
2025-01-15

Condition(s) studied

HysterectomyHysterectomy, Benign Uterine DiseasesHysterectomy, Vaginal

Investigational drug(s) / intervention(s)

vNOTESvaginal hysterectomy

vNOTES: vNOTES for benign hysterectomy

vaginal hysterectomy: vaginal hysterectomy for benign hysterectomy

Study summary

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

Sex
FEMALE
Min age
40 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * aged between 40 and 80 years * undergo hysterectomy for benign gynecological conditions Exclusion Criteria: * history of urogynecological surgery (including pelvic organ prolapse surgery and mid-urethral sling procedures), * suspected gynecologic malignancies, * endometriosis, * tubal-ovarian abscesses, * pelvic organ prolapse exceeding grade 2, * individuals who refused to participate in the study

Primary outcome measure(s)

  • the duration of surgery — The time from the beginning to the end of the operation
    İnterval from initial incision to the completion of vaginal cuff closure (minute)

Trial sites (1)

FacilityCityRegionStatus
Kartal Dr Lütfi Kirdar City Hospital Istanbul Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06776718 on ClinicalTrials.gov ↗ ← All trials in Turkey