Single Port Myomectomy Versus Conventional Myomectomy (SM)
|ClinicalTrials.gov Identifier: NCT01826578|
Recruitment Status : Unknown
Verified April 2013 by JungRyoel Lee, Seoul National University Hospital.
Recruitment status was: Not yet recruiting
First Posted : April 8, 2013
Last Update Posted : April 8, 2013
|Condition or disease||Intervention/treatment||Phase|
|Cosmetic Outcomes||Procedure: using only one port for laparoscopic surgery||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||106 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Prospective Randomized Controlled Trial to Analyze the Benefits of Single Port Laparoscopic Myomectomy in the View of Cosmetics and Patient Satisfaction|
|Study Start Date :||May 2013|
|Estimated Primary Completion Date :||September 2014|
|Estimated Study Completion Date :||December 2014|
|Experimental: single port arm||
Procedure: using only one port for laparoscopic surgery
using only one port for laparoscopic surgery
Other Name: Single port intervention
No Intervention: Conventional arm
Using 3-4 port for laparosocpic surgery
- Cosmetic benefits of single port laparoscopic myomectomy to conventional myomectomy in the view of scar evaluation [ Time Frame: for 8 weeks ]The characteristics of scar such as color, pliability, and stiffness are willing to be measured in 1 week and 8 week later after myomectomy. The level of satisfaction of patients will also be evaluated.
- Cosmetic benefits of single port laparoscopic myomectomy to conventional myomectomy in the view of patient satisfaction [ Time Frame: for 8 weeks ]Patient satisfaction about scar formation after myomectomy are willing to be evaluated after surgery.
- General composite characteristics of surgery procedure and outcome [ Time Frame: 1 week ]Composite parameters about surgery outcome and complication such as Op time, Drop of Hb, postop pain, duration of hospital stay, intraop complication, postop complication are willing to be measured.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01826578
|Contact: JungRyoel Lee, assistant firstname.lastname@example.org|
|Korea, Republic of|
|Seoul University Bundang Hospital OB & GY||Not yet recruiting|
|Sungnam-si, Kyeonggi-do, Korea, Republic of, 463-707|