Effect of preoperative anxiety on postoperative recovery quality of women with first and second cesarean sections

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200059113

Enrollment

Unknown

Registered

2022-04-25

Start date

2022-05-01

Completion date

Unknown

Last updated

2024-02-11

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

Conditions

Preoperative anxiety

Interventions

case series:None

Eligibility

Sex/Gender

Female

Age

18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Aged range from 18 to 35 years; 2. American Society of Anesthesiologists (ASA) grade I to II; 3. Full term pregnancy; 4. Maternal can complete the questionnaire independently or with the help of investigators and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1. Combined with eclampsia or preeclampsia; 2. Placenta previa; 3. Heart valve disease; 4. Cardiomyopathy; 5. Essential hypertension; 6. Premature labor or abnormal fetus requiring emergency caesarean section; 7. Have intellectual disability; 8. Contraindications of intraspinal anesthesia; 9. Refused to participate in the study.

Design outcomes

Primary

Measure	Time frame
State-trait anxiety inventory (STAI) score;Visual analogue scale for anxiety;	—

Secondary

Measure	Time frame
Heart rate;Systolic blood pressure;Diastolic blood pressure;Pulse oxygen saturation;Vasoactive drug dosage;Number of analgesic pump presses;Apgar score;Visual analogue scale pain score;Time to get out of bed;Time to start breastfeeding;Hospitalization days;	—

Countries

China

Contacts

Public ContactLi Junxiang

494973600@qq.com+86 18349301952

Outcome results

None listed

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