Circadian Rhythm Status and CS (Cesarean Section) Postoperative Pain
NCT ID: NCT05446636
Last Updated: 2024-08-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
280 participants
OBSERVATIONAL
2023-02-14
2025-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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Huawei bracelet
Huawei bracelet was used to continuously record maternal respiration, heart rate, temperature and sleep data, and then calculate maternal circadian rhythm state
Eligibility Criteria
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Inclusion Criteria
* 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 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
20 Years
45 Years
FEMALE
No
Sponsors
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The Second Affiliated Hospital of Chongqing Medical University
OTHER
Responsible Party
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Principal Investigators
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Guangyou Duan, MD
Role: STUDY_DIRECTOR
The Second Affiliated Hospital, Chongqing Medical University
Locations
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Department of Anesthesiology, The Second Affiliated Hospital, Chongqing Medical University
Chongqing, Chongqing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Biological rhythm and CS pain
Identifier Type: -
Identifier Source: org_study_id
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