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NCT07306507: VNOTES-TLH
vNOTES vs Laparoscopic Hysterectomy: Randomized Trial on Pain and Recovery"
NA trial testing vNOTES Hysterectomy in Hysterectomy in 90 participants. Completed in 10 April 2026.
9 April 2026
Quick facts
| Lead sponsor | Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 90 |
| Start date | 8 January 2026 |
| Primary completion | 9 April 2026 |
| Estimated completion | 10 April 2026 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- vNOTES Hysterectomy
- Total Laparoscopic Hysterectomy
Conditions studied
- Hysterectomy — all drugs for Hysterectomy →
Sponsor
Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
Who can join
Adults 18 to 75, female only, with Hysterectomy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study is a prospective, randomized controlled trial comparing two different minimally invasive hysterectomy techniques: vaginal natural orifice transluminal endoscopic surgery (vNOTES) and conventional total laparoscopic hysterectomy (TLH). The aim is to evaluate whether vNOTES provides better postoperative comfort and recovery by reducing pain, lowering opioid analgesic requirements, and improving early recovery outcomes. Approximately 80 women undergoing elective hysterectomy will be randomly assigned to either vNOTES or TLH. All surgeries will be performed under standardized general anesthesia by the same experienced surgical team. Postoperative pain management will follow an identical protocol for all patients. Primary outcomes include postoperative pain scores (at 12 and 24 hours) and total opioid consumption. Secondary outcomes include Quality of Recovery-15 (QoR-15) scores, fatigue scores, time to first mobilization, time to first flatus, and length of hospital stay. The results of this study may help identify which hysterectomy technique offers better patient-centered recovery and postoperative comfort.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07306507
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07306507 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
- Last refreshed: 15 April 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07306507.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing