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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01829022
Other study ID # NCCNCS-13-MAR
Secondary ID
Status Completed
Phase N/A
First received March 27, 2013
Last updated June 24, 2014
Start date April 2013
Est. completion date April 2014

Study information

Verified date June 2014
Source National Cancer Center, Korea
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Observational

Clinical Trial Summary

Primary objectives : To investigate technical feasibility and postoperative morbidity after E-NOTES for Myomectomy with Traction of Multidirectional Sutures

Secondary objectives : To investigate postoperative pain after E-NOTES for Myomectomy with Traction of Multidirectional Sutures by clinical variables such as incision size, type of port, size and number of myoma, or operation time.


Description:

- Leiomyoma is a common benign tumor of the smooth muscle cells of the myometrium.1 It can cause several symptoms such as abnormal vaginal bleeding, pain, or urinary symptoms according to size and location. Steadily, lesser invasive surgeries have been preferred for such benign disease (laparotomy, laparoscopy, and then single-port surgery).2,3

- However, these minimal approaches, laparoscopic morcellation of preoperatively suspicious leimyoma, have the potential risk of peritoneal seeding of postoperative diagnosed leiomyosarcoma in the pathological examination.4 Currently, safe morcellation is also required during myomectomy while using a lesser invasive surgical approach such as single-port surgery or natural orifice transumbilical endoscopic surgery (NOTES).

- During single-port surgery or embryonic NOTES (E-NOTES) via an umbilicus, handling of myoma into different directions could be quite a big challenge. Fortunately, myoma is enough hard to pull with string and has a tendency not to rupture during manipulation of these strings.

- These concepts lead to traction of anchoring sutures during E-NOTES for myomectomy applied in the current case. Safe morcellation could be guaranteed, because direction morcellation via an umbilicus is possible in an endobag.

- This useful and safe surgical approach needs to be confirmed in multi-centers in terms of feasibility and morbidity.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Women who are surgically candidate for myomectomy

- Age > 20 years

Exclusion Criteria:

- Contraindications for laparoscopic surgery and/or general anesthesia.

- Greater than five fibroids sized of 3cm or more

- Uterus extending beyond the umbilicus

- Major medical comorbidity or psychiatric illness, which could affect follow-up and/or compliance

- Patients undergoing concomitant complex surgical procedures at the time of myomectomy (such as resection of severe endometriosis etc.)

- Pregnancy

- Patients with any suggestion of malignancy in the pelvis

- Patients with cooperation of another main surgical procedures such as severe adhesiolysis or low anterior resection

- Patients who are severely anemic or who have significant medical conditions such as cardiac or pulmonary disease

- Patients who refuse to participate or give consent to the procedures

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
E-NOTES
Embryonic-Natural Orifice Transumbilical Endoscopic Surgery for Myomectomy with Traction of Multidirectional Sutures

Locations

Country Name City State
Korea, Republic of National Cancer Center Goyang Gyeonggi
Korea, Republic of National Cancer Center Koyang-si

Sponsors (24)

Lead Sponsor Collaborator
National Cancer Center, Korea Ajou University, Asan Medical Center, CHA University, Cheil General Hospital and Women’s Healthcare Center, Ewha Womans University Mokdong Hospital, Hallym University Medical Center, Hanyang University, Incheon St.Mary's Hospital, Inje University, Keimyung University Dongsan Medical Center, Korea University Anam Hospital, Korea University Guro Hospital, Kyung Hee University Hospital at Gangdong, Kyungpook National University, National Health Insurance Service Ilsan Hospital, Pusan National University Yangsan Hospital, Saint Vincent's Hospital, Korea, Samsung Medical Center, Seoul National University Bundang Hospital, Seoul National University Hospital, Severance Hospital, Soonchunhyang University Hospital, The Catholic University of Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Technical feasibilities and postoperative morbidity after E-NOTES for Myomectomy with Traction of Multidirectional Sutures Technical feasibility and postoperative morbidity will be evaluated in terms of overall or institutional conversion rate to convetional multi-port laparoscopy or laparotomy, operation time for each surgical procedures: dissection, morecellation, suturing, and total surgical procedures, complication, change of hemoglobin, and estimated blood loss Postoperative surveillance including pain evaluation as routine clinical practise for 1 months Yes
Secondary Postoperative pain after E-NOTES for Myomectomy with Traction of Multidirectional Sutures by clinical variables such as incision size, type of port, size and number of myoma, or operation time. Visual analogue scale will be used for pain evaluation: preoperative, postoperative 24 hour, postoperative 48 hour, postoperative 10 day (7 to 10 day), and postoperative 28 day (21 to 35 day). Preoperative and postoperative pain No
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