A randomized, placebo controlled, trial of preoperative sustained release betamethasone plus non-controlled intraoperative ketorolac or fentanyl on pain after diagnostic laparoscopy or laparoscopic tubal ligation

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN52633712

Enrollment

Registered

2003-08-19

Start date

2002-01-01

Completion date

Unknown

Last updated

2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative pain Signs and Symptoms Pain

Interventions

Sustained release betamethasone versus placebo.

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing laparoscopic surgery at University of Tennessee Medical Centre Knoxville, Tennessee (USA)

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

Measure	Time frame
Not provided at time of registration	—

Secondary

Measure	Time frame
Not provided at time of registration	—

Countries

United States of America

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026