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Clinical Trial on Opioid-Free Anesthesia Protocol for Reducing the Incidence of Postoperative Nausea and Vomiting in Gastrointestinal Cancer Surgery

Randomized Controlled Trial of Opioid-Free Anesthesia Protocol for Reducing the Incidence of PONV in Gastrointestinal Cancer Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105827
Enrollment
Unknown
Registered
2025-07-11
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Postoperative Nausea and Vomiting

Interventions

The opioid-free anesthesia group:General anesthesia (without the use of opioid drugs)+PCEA
Normall opioid anesthesia group:General anesthesia (using opioid drugs)+PCEA

Sponsors

The Seventh Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) The participant and/or their legally authorized representative voluntarily provide written informed consent for this trial. (2) Age between 18 and 65 years, inclusive (18 = 3 points). (5) Scheduled to undergo laparoscopic surgery for gastric or colorectal tumors.

Exclusion criteria

Exclusion criteria: (1) Severe impairment of major organ functions (including cardiac, hepatic, cerebral, pulmonary, or renal systems). (2) Elevated intraocular or intracranial pressure. (3) Contraindications to neuraxial anesthesia (e.g., coagulopathy or history of thoracic spine trauma). (4) Chronic opioid use or pre-existing chronic pain disorders. (5) Known allergies or contraindications to the study medications. (6) Other conditions deemed clinically unsuitable for participation by the investigator.

Design outcomes

Primary

MeasureTime frame
The incidence of postoperative nausea and vomiting (PONV) in patients 72 hours after the operation;

Secondary

MeasureTime frame
The QoR-15 scale of the patient before the operation, 24 hours after the operation and 48 hours after the operation;Postoperative extubation time;The degree of pain experienced by the patient after the operation;The incidence of postoperative hypotension;The time for postoperative patients to resume defecation and passing gas;The incidence of postoperative skin itching;Length of hospital stay for the patient;

Countries

China

Contacts

Public ContactChi Xinjin

The Seventh Affiliated Hospital, Sun Yat-sen University

chixinjin@sysush.com+86 189 2340 9020

Outcome results

None listed

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