← Eichor
Study identifier: NCT07467577 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Does Intraperitoneal Washout Further Reduce Pain After Low-Pressure vNOTES Hysterectomy?

Condition: Postoperative Pain · vNOTES  ·  Sponsor: Erzincan Military Hospital

PhaseNA
Planned participants94
Who can joinFemale, 18 Years to 80 Years
Healthy volunteersYes

About this study

The evolution of minimally invasive gynecology has transitioned from traditional laparotomy to laparoscopy, and most recently, to vNOTES (Vaginal Natural Orifice Transluminal Endoscopic Surgery). By combining the visual advantages of endoscopy with the scarless approach of vaginal surgery, vNOTES has demonstrated superior outcomes in terms of reduced postoperative pain, shorter hospital stays, and improved cosmetic results compared to traditional total laparoscopic hysterectomy (TLH). Despite these advancements, post-laparoscopic pain syndrome (PLPS) remains a significant clinical challenge. Characterized by deep-seated abdominal pressure and referred shoulder-tip pain, PLPS is primarily attributed to the irritation of the phrenic nerve caused by residual carbon dioxide and the formation of carbonic acid on the peritoneal surface. In the Trendelenburg position required for gynecologic procedures, this gas often becomes trapped in the subdiaphragmatic space, leading to significant distress that can delay discharge even when the surgical site itself is healing well. The physiological impact of the pneumoperitoneum is largely pressure-dependent. The landmark study by Barczyński and Herman (2004) in general surgery established that maintaining a low-pressure pneumoperitoneum (\<10 mmHg) significantly reduces peritoneal stretching and the subsequent inflammatory response. Furthermore, the technique of intraperitoneal saline washout has been proposed to physically remove residual…

This description comes directly from the study's public registry record.

Talk to the study team

Kemal GUNGORDUK  ·  +905054921766  ·  drkemalgungorduk@gmail.com

Always discuss trial participation with your own doctor first.

Locations (2)

Mugla Education and Research HospitalMuğla, Turkey (Türkiye)Recruiting
Muğla Sıtkı Kocman UniversityMuğla, Turkey (Türkiye)Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07467577