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Effects of Perioperative Intravenous Dexamethasone on Pain in Out Patient Knee Surgery

Beth Israel Lahey Health logo

Beth Israel Lahey Health

Status and phase

Terminated
Phase 4

Conditions

Nausea
Post Operative Pain

Treatments

Drug: placebo
Drug: Dexamethasone 8mg iv x1

Study type

Interventional

Funder types

Other

Identifiers

NCT01149616
2009P000345

Details and patient eligibility

About

The purpose of the study is to determine the opiate sparing effects of intravenously administered dexamethasone in outpatient knee surgery. Dexamethasone is a glucocorticoid with well known antiemetic effects. However, the analgesic effects of dexamethasone have not been adequately researched. Following surgery, patients are typically discharged home with PO opiates to manage post-operative pain. The investigators believe that by using VAS (Visual Analog Scale) for Pain the investigators can show that a single dose of dexamethasone can reduce pain scales and opiate consumption post-operatively, on Post Operative Day (POD 1) when compared to placebo.

Full description

Findings of Modest improvement in pain scores and postoperative nausea at 24 hours with Dexamethasone

Enrollment

82 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult patients undergoing ambulatory knee arthroscopy surgery
  • Must provide phone contact number and agree to phone followup on post operative day 1

Exclusion criteria

  • Patients with major systemic disease
  • Allergy or intolerance to study drug

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

82 participants in 2 patient groups, including a placebo group

Intervention
Active Comparator group
Description:
Dexamethasone 8mg iv x 1
Treatment:
Drug: Dexamethasone 8mg iv x1
Placebo
Placebo Comparator group
Description:
placebo
Treatment:
Drug: placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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