NCT02150239

Brief Summary

Pain management is becoming an important ethical responsibility of the medical profession and a focus of the health care system. However, there are limited literature evaluate the postoperative pain experience and management in our local setting.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
250

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2014

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2014

Completed
25 days until next milestone

First Submitted

Initial submission to the registry

May 26, 2014

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 29, 2014

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2014

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2014

Completed
Last Updated

June 10, 2014

Status Verified

June 1, 2014

Enrollment Period

4 months

First QC Date

May 26, 2014

Last Update Submit

June 9, 2014

Conditions

Postoperative Pain

Keywords

painpostoperative

Outcome Measures

Primary Outcomes (1)

  • postoperative pain experience

    To determine patient's postoperative pain experience during and 2 weeks after discharge from hospital.

    2 weeks

Study Arms (1)

postoperative pain

Procedure: operation

Interventions

operationPROCEDURE
postoperative pain

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult with age ≥ 18 who undergo operation

You may qualify if:

  • \. Adult with age ≥ 18 who undergo operation

You may not qualify if:

  • \. Refused to give informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Malaya Medical Center

Kuala Lumpur, KL, 59100, Malaysia

RECRUITING

MeSH Terms

Conditions

Pain, PostoperativePain

Interventions

Surgical Procedures, Operative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsNeurologic ManifestationsSigns and Symptoms

Study Officials

  • Wang Chew Yin

    University of Malaya

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Prof Wang Chew Yin

CONTACT

03-79492052wangcy@um.edu.my

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Target Duration
2 Weeks
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 26, 2014

First Posted

May 29, 2014

Study Start

May 1, 2014

Primary Completion

September 1, 2014

Study Completion

November 1, 2014

Last Updated

June 10, 2014

Record last verified: 2014-06

Locations

MY(1)