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Circadian Rhythm Status and CS (Cesarean Section) Postoperative Pain

C

Chongqing Medical University

Status

Enrolling

Conditions

Circadian Rhythm

Treatments

Device: Huawei bracelet

Study type

Observational

Funder types

Other

Identifiers

NCT05446636
Biological rhythm and CS pain

Details and patient eligibility

About

Use huawei wristwatch to record maternal rhythm status and record the VAS score after cesarean section under combined spinal-epidural anesthesia. Based on this study the investigators intend to explore the correlation between maternal circadian rhythm status and postoperative pain after cesarean section.

Enrollment

280 estimated patients

Sex

Female

Ages

20 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 20 to 45
  • ASA(American society of anesthesiologists) status II-III
  • 37-42 weeks gestation
  • undergo elective cesarean section with subarachnoid anesthesia
  • participate in this study and sign informed consent

Exclusion criteria

  • Patients with contraindications of combined spinal and epidural anesthesia
  • Patients with severe systemic disease
  • Alcoholism and long-term use of anti-inflammatory and analgesic drugs
  • Patients who were unable to cooperate or refused to participate in the trial
  • with psychiatric disorder
  • researchers considered unsuitable to participate in or unable to cooperate with the study

Trial contacts and locations

1

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Central trial contact

HUANG HE, MD

Data sourced from clinicaltrials.gov

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