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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01093430
Other study ID # AM2009/1
Secondary ID
Status Recruiting
Phase N/A
First received March 23, 2010
Last updated March 24, 2010
Start date September 2009
Est. completion date September 2011

Study information

Verified date March 2010
Source Royal Free Hampstead NHS Trust
Contact Adam Magos, MD FRCOG
Phone 020 7794 0500
Email a.magos@medsch.ucl.ac.uk
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to study port symmetry and the incidence of anterior abdominal wall neuropathy associated with gynaecological surgery.


Description:

We plan to study patients undergoing gynaecological laparoscopy. Patients will be randomized to two techniques for determining where to position the right and left lateral laparoscopic ports, and port symmetry will be assessed at the end of surgery. We also plan to study patients undergoing any type of gynaecological surgery to determine the incidence of sensory neuropathy involving the lower abdomen according to the route of surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date September 2011
Est. primary completion date September 2011
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 55 Years
Eligibility Inclusion Criteria:

- Due to undergo elective gynaecological surgery, including laparoscopy

Exclusion Criteria:

- Previous laparoscopy

- Junior intern as primary surgeon

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Anterior superior iliac spine
The position of the right and left laparoscopic port sites will be determined by palpation of the nearby anterior superior iliac spine of the pelvic bone.
Control
The position of the right and left laparoscopic port sites will be determined by visual inspection of the anterior abdominal wall.

Locations

Country Name City State
United Kingdom Royal Free Hospital London

Sponsors (1)

Lead Sponsor Collaborator
Royal Free Hampstead NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Symmetry of lateral laparoscopic ports The precise location in the horizontal and vertical planes of the right and left lateral port sites will be measured to assess port symmetry. On the completion of laparoscopy and before the general anaesthetic is reversed No
Secondary Neuropathy Evidence of ilio-hypogastric and ilio-inguinal neuropathy will be sought at the above time frames. Before, immediately after and 2 weeks after gynaecological surgery No
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