NCT05624502

Brief Summary

This is an observational study project aims at improving postoperative pain outcomes by evaluating the current status of postoperative pain managements in the institution. Then the investigators will compare the results by internal and external benchmarking. Then they will suggest recommendations to improve the current situation of postoperative pain management.

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
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2019

Longer than P75 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

January 1, 2019

Completed
3.9 years until next milestone

First Submitted

Initial submission to the registry

November 13, 2022

Completed
9 days until next milestone

First Posted

Study publicly available on registry

November 22, 2022

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

December 27, 2022

Status Verified

December 1, 2022

Enrollment Period

5.8 years

First QC Date

November 13, 2022

Last Update Submit

December 22, 2022

Conditions

Acute Post Operative Pain

Keywords

acute postoperative painorthopedic surgerygeneral surgeryobs/gyn surgeryNeurosurgeryBariatric surgeryThoracic surgeryopioidsNSAIDsRegional analgesia

Outcome Measures

Primary Outcomes (3)

  • postoperative pain scores

    using visual analogue scale (VAS) for pain assessment of 11 points (from "0" no pain to "10" worst pain

    first 3 days postoperative

  • time in severe pain

    duration of time spent in severe pain after surgery

    during the first 24 hours

  • dynamic and static pain

    Pain scores or rest and during movements

    during the first 24 hours

Secondary Outcomes (3)

  • worst and least pain

    during the first 24 hours

  • time to first request of analgesia

    during the first 24 hours

  • total analgesic consumption

    during the first 24 hours

Eligibility Criteria

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

Acute postoperative pain patients after different surgical procedures

You may qualify if:

  • Postoperative patients during the first 24 hours of surgery (day 1)
  • Male and Females
  • Adults

You may not qualify if:

  • Patient refusal
  • Drug abusers and addicts
  • Major significant systemic diseases
  • Language barriers

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Salah N. El-Tallawy

Riyadh, 7805, Saudi Arabia

RECRUITING

MeSH Terms

Conditions

Pain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor and Consultant - Anesthesia and Pain Management

Study Record Dates

First Submitted

November 13, 2022

First Posted

November 22, 2022

Study Start

January 1, 2019

Primary Completion

October 31, 2024

Study Completion

December 31, 2024

Last Updated

December 27, 2022

Record last verified: 2022-12

Data Sharing

IPD Sharing
Will not share

Locations

SA(1)