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Establishment and evaluation of maternal comfort scale in convalescent period after cesarean section

Establishment and evaluation of maternal comfort scale in convalescent period after cesarean section

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100053057
Enrollment
Unknown
Registered
2021-11-10
Start date
2022-02-14
Completion date
Unknown
Last updated
2022-09-06

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

Conditions

Postpartum comfort

Interventions

Case series:None

Sponsors

West China Second Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. ASA 1-3, cesarean delivery; 2. Have a clear consciousness and be able to complete the scale survey by themselves or with the help of others; 3. Voluntarily participate in the investigation and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pregnant women who plan to enter the ICU after operation and use sedation without communication; 2. Pregnant women with mental disorders or communication barriers; 3. Cesarean section due to induced labor or stillbirth; 4. Serious accidental complications during anesthesia; 5. Violation of clinical trial protocol (e.g. loss of follow-up for more than 3 consecutive times, preoperative discharge of patients or cancellation of surgery).

Design outcomes

Primary

MeasureTime frame
Maternal comfort index;—

Countries

China

Contacts

Public ContactZuo Yunxia, Shu Lijuan

West China Second Hospital of Sichuan University

czshulj2009@163.com+86 15828122180, +86 18980601541

Outcome results

None listed

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