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Improvement in Postoperative Pain Outcomes

Mprovement in Postoperative Pain Outcome: Pain Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05624502
Enrollment
1000
Registered
2022-11-22
Start date
2019-01-01
Completion date
2024-12-31
Last updated
2022-12-27

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

Conditions

Acute Post Operative Pain

Keywords

acute postoperative pain, orthopedic surgery, general surgery, obs/gyn surgery, Neurosurgery, Bariatric surgery, Thoracic surgery, opioids, NSAIDs, Regional analgesia

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.

Detailed description

At least half of the patients suffer from moderate to severe post-operative pain. The price of poorly managed pain is high: pain impedes recovery, causes suffering and prolongs the hospital stay. PAIN OUT provides tools for measurement, feedback and benchmarking of pain treatment quality in order to improve patient care. A research project that aims at improving postoperative pain treatment outcomes by evaluating the current status of postoperative pain managements in our institution. Then the investigators compare the results by internal and external benchmarking. Then suggest recommendations to improve the current situation of postoperative pain management. parameters include Patient's data Pain assessments by using the visual analogue score of 11 point (from 0 no pain - 10 worst pain) will be evaluated as the following: Worst pain since surgery, Least pain since surgery, Pain score at rest. Pain score during movements in bed, Pain score during deep breathing and coughing, How often the severe pain since surgery (%), Does the pain interfere with sleeping pattern, and the side effects.

Interventions

None listed

Sponsors

King Saud University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
postoperative pain scoresfirst 3 days postoperativeusing visual analogue scale (VAS) for pain assessment of 11 points (from 0 no pain to 10 worst pain
time in severe painduring the first 24 hoursduration of time spent in severe pain after surgery
dynamic and static painduring the first 24 hoursPain scores or rest and during movements

Secondary

MeasureTime frameDescription
worst and least painduring the first 24 hoursThe highest and lowest pain scores during the first 24 hours
time to first request of analgesiaduring the first 24 hoursthe time from the recovery to the first request of postoperative analgesia
total analgesic consumptionduring the first 24 hourstotal consumption of opioids / non-opioids during the first 24 hours

Countries

Saudi Arabia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026