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OpenTrials
Completed

NCT Number: NCT01418807

Transumbilical Versus Transvaginal Specimen Retrieval at Minilaparoscopy

We hypothesise that pain at minilaparoscopy for gynecologic disease is reduced when transvaginal rather than transumbilical specimen extraction is accomplished. This would be due to the avoidance of a 10-mm port in the umbilicus. Visual analogue scale score of post-operative pain will be obtained and patients satisfaction will be asked at the 2-month postoperative visit.

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Key information

Conditions

Postoperative Pain Intraoperative Complications Neurologic Manifestations Pain Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Patients Satisfaction Postoperative Complications Signs and Symptoms

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Department of Obstetrics and Gynecology Universita' Dell'Insubria

Varese, 21100, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adnexal Mass
  • Benign Gynecologic Condition
  • Laparoscopicb Surgery

Exclusion criteria

  • Obliteration Of The Douglas Pouch

Treatment and study plan

TRANSVAGINAL SPECIMEN EXTRACTION

Procedure

Transvaginal specimen retrieval following posterior colpotomy

TRANSUMBILICAL SPECIMEN EXTRACTION

Procedure

Transumbilical specimen retrieval following enlargement of the umbilical port

Primary outcomes

  1. Postoperative Pain

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Università degli Studi dell'Insubria

Other

Registry information

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
Aug 17, 2011
Registry last updated
Feb 24, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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