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The reliability of various preoperative pain assessment methods in predicting the degree of acute pain after cesarean section

The reliability of various preoperative pain assessment methods in predicting the degree of acute pain after cesarean section

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048341
Enrollment
Unknown
Registered
2021-07-05
Start date
2021-07-15
Completion date
Unknown
Last updated
2022-03-14

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

Conditions

Acute postoperative pain

Interventions

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Sponsors

Hejiang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1.Pregnant women aged 20 to 35 years (excluding the influence of low age and advanced age); 2.Full-term pregnancy (>=37 weeks); 3.Body mass index 18-30kg/m^2; 4.Plan to choose intraspinal anesthesia; 5.Coagulation function and platelet normal, no spinal deformity And trauma, no other contraindications to intraspinal anesthesia; 6.Agree to participate in clinical trials and sign informed consent; 7.Agree to use postoperative intravenous self-controlled analgesia pump (PCIA).

Exclusion criteria

Exclusion criteria: 1.Pregnancy-induced hypertension and its complications; 2.Women with underlying diseases before pregnancy; 3.Cesarean section under general anesthesia; 4.Failure of peripheral venous catheterization (failure of repeated puncture twice); 5.Women who cannot cooperate with the study; 6.Women with perinatal hemorrhage 7.The operation time is greater than 2 hours; 8.The fetus has moderate to severe asphyxia; 9.The data collection cannot be completed due to time constraints; 10.The data record is not perfect; 11.The PCIA is stopped early 24 hours after the operation.

Design outcomes

Primary

MeasureTime frame
Pain score during resting and exercise at various time points within 48 hours after surgery;Self-controlled analgesia pump first compression time;Number of compressions within 24 hours and 48 hours after the operation of the self-controlled analgesia pump;

Secondary

MeasureTime frame
Regression of the level of anesthesia in the spinal canal;Number of mothers with remedial analgesia;

Countries

China

Contacts

Public ContactWang Tihe

Hejiang People's Hospital

wangtihes@qq.com+86 13890419317

Outcome results

None listed

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