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Effect of Preoperative Information About Pain on Postoperative Pain Experience and Patient Satisfaction

NCT03056521 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 340

Last updated 2017-02-17

No results posted yet for this study

Summary

Patients are randomized into 2 groups. The intervention group which receives preoperative counseling about pain and a control group which does not receive this counseling.

The patients are followed up looking at pain scores and pain experience and satisfaction with pain management for 2 days post operative.

Conditions

  • Post Operative Pain

Interventions

OTHER

preoperative information about pain

It is information about analgesics, post operative pain, complications of pain, benefits of pain treatment and non pharmacologic treatment options.

Sponsors & Collaborators

  • Makerere University

    lead OTHER

Principal Investigators

  • Moses Othin · Makerere University College of Health Sciences

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2017-02-28
Completion
2017-03-31

Countries

  • Uganda

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03056521 on ClinicalTrials.gov