About this trial
To assess the effect of intraperitoneal drain placement on postoperative pain after Gynecologic laparoscopy To evaluate whether the use of drains contributes to improved other clinical outcomes
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Elective procedure: Patients scheduled for elective pure laparoscopic gynecologic surgery (e.g., ovarian cystectomy, endometriosis resection, diagnostic laparoscopy).
ASA Physical Status: I-II (i.e., healthy or mild systemic disease).
Disqualifiers
None
Trial population
The study population will consist of women undergoing elective laparoscopic gynecologic surgery at \[Insert Hospital/Institution Name\] over a \[insert duration, e.g., 6-month or 12-month\] period. Eligible participants will be adult females aged 18 to 65 years who are scheduled for non-oncologic, minimally invasive gynecologic procedures such as ovarian cystectomy, salpingectomy, diagnostic laparoscopy, or laparoscopic management of endometriosis.
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Corelation between intraperitoneal drain placement and Postoperative pain in Gynecologic laparoscopy
Evalute post operative pain levels and discomfort through Visual Analouge Scale (VAS) score
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: