Clinical Trials Directory

Trials / Unknown

UnknownNCT01433874

Decreasing Upper and Shoulder Pain After Laparoscopic Surgery

Maneuvers to Decrease Upper and Shoulder Pain After Gynecologic Laparoscopic Surgery

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Taipei Veterans General Hospital, Taiwan · Other Government
Sex
Female
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Laparoscopic surgery is becoming a major procedure, owing to smaller incisions, shorter hospitalizations, and less post-operative pain as compared with traditional laparotomies. However, there is marked interindividual variability of post-operative shoulder-tip pain following laparoscopic surgery. The incidence of shoulder pain varies from 35% to 80% and ranges from mild to severe. In some cases, it has been reported to last more than 72 hours after surgery. The hypothesis of post-operative shoulder-tip pain is that carbon dioxide induced phrenic nerve irritation causes referred pain to C4. Therefore, the investigators should try to do is that if the investigators could reduce carbon dioxide retention in the pelvic cavity. This clinical controlled trial is tried to find out the practical and clinical maneuver to reduce post-operative should-tip pain following laparoscopic surgery.

Detailed description

This clinical controlled trial is tried to find out the practical and clinical maneuver to reduce post-operative upper abdominal and shoulder pain after laparoscopic surgery.

Conditions

Interventions

TypeNameDescription
PROCEDUREPulmonary recruitment maneuverA pulmonary recruitment maneuver consisting of five manual pulmonary inflations was performed with a maximum pressure of 60 cmH2O. The anesthesiologist held the fifth positive pressure inflation for approximately 5 seconds.
PROCEDUREIntraperitoneal normal saline infusionThe upper part of the abdominal cavity was evenly and bilaterally filled with the 0.9% normal saline in the amount of 500cc. We will leave the fluid in the abdominal cavity
PROCEDUREcombined groupThe upper part of the abdominal cavity was evenly and bilaterally filled with the 0.9% normal saline in the amount of 500cc. Later, a pulmonary recruitment maneuver consisting of five manual pulmonary inflations was performed with a maximum pressure oof 60 cmH2O.
PROCEDUREControl groupCo2 was removed by passive exsufflation through the port site.

Timeline

Start date
2011-02-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2011-09-14
Last updated
2011-09-14

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT01433874. Inclusion in this directory is not an endorsement.