A Retrospective Review Of Outcomes Following Laparoscopic Myomectomy

Laparoscopic Myomectomy Clinical Trial

— retromyo  

Official title:

A Retrospective Review Of Outcomes Following Laparoscopic Myomectomy

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00672750
• Other study ID #: 23597
• Status: Terminated
• Phase: N/A
• First received: May 1, 2008
• Last updated: January 24, 2017
• Start date: February 2008
• Est. completion date: September 16, 2016

Study information

• Verified date: January 2017
• Source: The Advanced Gynecologic Surgery Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This will be a retrospective review of approximately 900 patients who have undergone laparoscopic myomectomy since 1999. patients will be contacted by phone and surveyed. All patients who have had laparoscopic myomectomy will be included. Only those not wishing to take part in the survey will be excluded. The data will then be compiled for statistical analysis , looking at pain, bleeding and subsequent fertility.

Description:

Patients will be called and surveyed using a survey tool. They will be asked about what factors lead them to have surgery and then was their issue resolved after surgery.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 70
• Est. completion date: September 16, 2016
• Est. primary completion date: September 16, 2016
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 16 Years to 70 Years

Eligibility

Inclusion Criteria:

• All patients who are willing to be surveyed

Exclusion Criteria:

• Those patients who are not willing to answer the survey will be excluded

• Those patients who are unable to be contacted( ie; moved) will be excluded

Related Conditions & MeSH terms

• Laparoscopic Myomectomy

Locations

Country	Name	City	State
United States	Advanced Gynecologic Surgery Institute	Naperville	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
The Advanced Gynecologic Surgery Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	That patients who had pain prior to laparoscopic myomectomy will have less pain in 75% of the cases		since 1999
Secondary	That patients who had menorrhagia prior to laparoscopic myomectomy would see a reduction after surgery 75% of the time		since 1999