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Study of Laparoendoscopic Single Site Adnexal Surgery for Benign Ovarian and Tubal Disease

Not Applicable
Conditions
Benign Ovarian or Tubal Disease
Interventions
Procedure: Three-port laparoscopic adnexal surgery
Procedure: Single-port laparoscopic adnexal surgery
Registration Number
NCT01679509
Lead Sponsor
Asan Medical Center
Brief Summary

To compare the safety and efficacy between single-port and three-port adnexal surgery in patients with benign ovarian and tubal disease

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
330
Inclusion Criteria
  • Patient who undergo laparoscopic adnexal surgery due to following benign adenxal disease

    1. Benign teratoma
    2. Endometrioma
    3. Mucinous cystadenoma
    4. Serous cystadenoma
    5. Benign Brenner tumor
    6. Ectopic pregnancy(cornual, tubal, ovarian pregnancy, etc.)
    7. paratubal cyst, parovarian cyst
    8. Risk reducing bilateral salpingooophorecotmy due to familial breast/ovarian cancer syndrome
    9. Other benign adnexal disease requiring surgery
  • American Society of Anesthesiologist Physical Status classification I-II.

  • Patient who have signed written informed consent

Exclusion Criteria
  • Uncontrolled medical disease
  • Active infectious disease
  • Previous pelvic radiation therapy
  • Patient who requires further procedure excluding adnexal surgery
  • Patient who has other pain source excluding adnexal disease
  • Pregnant and lactating woman

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Three-port surgery groupThree-port laparoscopic adnexal surgeryThree-port laparoscopic adnexal surgery
Single-port surgery groupSingle-port laparoscopic adnexal surgerySingle-port laparoscopic adnexal surgery
Primary Outcome Measures
NameTimeMethod
postoperative hospital staywithin 1 week after surgery
Secondary Outcome Measures
NameTimeMethod
postoperative painwithin 1 week after surgery
postoperative analgesics requirementwithin 1 week after surgery
quality of lifewithin 6 months aftr surgery
surgical stress responsewithin 2 days after surgery
operating timeimmediately ater surgery
transfusion requirement and amountwithin 1 week after surgery
postoperative complicationwithin 1 months after surgery

Trial Locations

Locations (1)

Department of Obstetrics and Gynecology, Universit of Ulsan College of Medicine, Asan Medical Center

🇰🇷

Seoul, Korea, Republic of

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