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The effect of predictive opioid-sparing analgesia protocol on recovery of gastrointestinal function after colorectal surgery: a randomized controlled trial

The effect of predictive opioid-sparing analgesia protocol on recovery of gastrointestinal function after colorectal surgery: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039672
Enrollment
Unknown
Registered
2020-11-05
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-02-16

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

Conditions

recovery of gastrointestinal function after colorectal surgery

Interventions

predictive opioid-sparing analgesia group:a pre-operative multimodal sparing-opioid analgesia based on pain risk prediction
conventional analgesia group:conventional peri-operative multimodal analgesia

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients who received colorectal surgeries and signed informed consent for the follow-up, body mass index between 18 and 30, American Society of Anesthesiology (ASA) grading between I and III.

Exclusion criteria

Exclusion criteria: 1. Patients signed informed consents before surgery but rejected participation for follow-up; 2. Intra-operative cardiac arrest, peri-operative mental diseases; 3. Pregnancy, patients who could not be extubated 2 hours after surgery.

Design outcomes

Primary

MeasureTime frame
I-FEED scoring system;

Secondary

MeasureTime frame
time to flatuence;time to feeding;acute post-operative pain;post-operative major complications;

Countries

China

Contacts

Public ContactPeng Lihua

The First Affiliated Hospital of Chongqing Medical University

plhbest@163.com+86 13983985210

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026