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Effect of preoperative frailty on postoperative pain in patients undergoing laparoscopic surgery

Effect of preoperative frailty on postoperative pain in patients undergoing laparoscopic surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060988
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

Pain

Interventions

No frailty group:No

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Aged>=18 years; 2.American Society of anesthesiologists (ASA) grade 1~3; 3.Patients scheduled for laparoscopic surgery; 4.Operation time >1 hour and <5 hours; 5.In line with the ethics, the patients volunteered and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1.A history of mental illness or long-term use of psychotropic drugs (dementia, schizophrenia), chronic analgesics and alcoholism; 2.Patients with severe cognitive impairment diagnosed by MMSE score less than 17; 3.Opioid allergy or preoperative opioid treatment for pain; 4.Patients with signs of neuropathic pain or taking neuropathic pain drugs before surgery; 5.Insensitivity to pain or hyperalgesia; 6.Cardiac insufficiency: NYHA>= grade 3 or echocardiography showed EF28kg/m2; 11.Language communication barrier, hearing barrier, unable to complete the properative evaluation test; 12.Allergic to narcotic drugs or other contraindications.

Design outcomes

Primary

MeasureTime frame
The incidence, severity and duration of pain during hospitalization;

Countries

China

Contacts

Public ContactXie Keliang

Tianjin Medical University General Hospital

mzk2011@126.com+86 15332112099

Outcome results

None listed

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