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Study on the prediction of acute pain after cesarean section

Study on the prediction of acute pain after cesarean section

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100042883
Enrollment
Unknown
Registered
2021-01-31
Start date
2021-02-05
Completion date
Unknown
Last updated
2021-05-17

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

Conditions

Acute pain after cesarean section

Interventions

Gold Standard:Clinical outcome
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Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Pregnant women undergoing cesarean section under spinal anesthesia; 2. ASA I-III; 3. Comply with the ethical requirements of patients to voluntarily accept signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Preoperative combined with cognitive dysfunction,preoperative hypoesthesia loss, abnormal pain experience and other symptom; 2. Preoperative psychoneurotic disease, unable to cooperate; 3. Critical condition, severe liver and kidney dysfunction; 4. Who was admitted to the ICU after surgery and no follow-up; 5. Patients enrolled in other clinical studies within 3 months; 6. Other circumstances that the investigator considers inappropriate for participation in the study.

Design outcomes

Primary

MeasureTime frame
Intolerance pain;Preoperative depression;Pain catastrophizing scale;SEN, SPE, ACC, AUC of ROC, PV+, PV-;

Countries

China

Contacts

Public ContactZongbin Song

Xiangya Hospital, Central South University

Songzb2001@163.com+86 13787246060

Outcome results

None listed

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