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OpenTrials
Completed

NCT Number: NCT01940042

the Effect of Simple Clinical Maneuver on Shoulder and Abdominal Pain a Laparascopic Gynecological Surgery:a Prospective Randomised Trial

The investigators think that a simple maneuver at laparascopic surgery to reduce the postoperative pain.

Completed

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Key information

Age range

15 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Tepecik Education and Research Hospital

Izmir, 35120, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • females aged 15-65 years,
  • American Society of Anesthesiologists (ASA) physical status classification I-III
  • no previous laparotomy(major abdominal surgery).
  • need a laparascopic surgery

Exclusion criteria

  • required hospitalization after the laparoscopic surgery,
  • the procedure required conversion to laparotomy
  • if a 48-hour follow-up was not feasible

Treatment and study plan

CO2 was removed by means of trandelenburg positions

Behavioral

Primary outcomes

  1. postoperative 12. hour VAS pain score

    Time frame: 12 hour

Secondary outcomes

  1. postoperative analgesic requırements

    Time frame: 48 hours

Other outcomes

  1. postoperative shoulder pain score

    Time frame: 7 days

Sponsors and collaborators

Lead sponsor

Istanbul Bakirkoy Maternity and Children Diseases Hospital

Other Gov

Registry information

Important dates

Study start
2013
Primary completion
2017
Study completion
2017
First posted
Sep 11, 2013
Registry last updated
Sep 5, 2018

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

View the official ClinicalTrials.gov record (opens in a new tab)

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.