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Opioid-free anesthesia in laparoscopic surgery: a randomized controlled trial

Opioid-free anesthesia in laparoscopic surgery: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021223
Enrollment
Unknown
Registered
2019-02-02
Start date
2019-02-11
Completion date
Unknown
Last updated
2021-09-20

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

Conditions

Disease that an abdominal surgery is needed

Interventions

OFA group:Opioid free anethesia
OA group:Traditional anethesia

Sponsors

The Fourth Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients aged from 18 to 65 years and scheduled for an abdominal surgery with the ASA status I/II, and Willing to sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with cerebrovascular disease, peptic ulcer,dysfunction of liver, renal dysfunction,diabetes, hematological system disorders; 2. History of chronic pain, long time of taking opioids,NSAIDS or hormones; 3. Allergic to local anesthetic; 4. Pregnant and lactating women; 5. Patients with mental disease who is unable to give a VAS score; 6. Regional nerve block contraindication; 7. patients with moderate or severe cardiopulmonary dysfunction; 8. patients with atropin contraindications.

Design outcomes

Primary

MeasureTime frame
Pain evaluation;Exhaust time;Nausea and vomiting postoperative;SaO2;

Secondary

MeasureTime frame
MAP;Length of stay;PaO2;blood glucose;Lactic acid;pH;potassium;

Countries

China

Contacts

Public ContactZhao Xuelian

The Fourth Hospital of Hebei Medical University

1400267824@qq.com+86 18531116096

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026