Anesthesia satisfaction survey of elective cesarean section with intrathecal morphine in patients who received combined spinal and epidural anesthesia for previous cesarean section.

Anesthesia satisfaction survey of elective cesarean section with intrathecal morphine in patients who received combined spinal and epidural anesthesia for previous cesarean section. - Anesthesia satisfaction survey for cesarean section.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000050980

Enrollment

Registered

2023-05-02

Start date

2022-09-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

cesarean section

Interventions

None listed

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1) Patients undergoing cesarean section under spinal anesthesia. 2) Patients whose previous cesarean section anesthesia was spinal epidural combined anesthesia and whose postoperative analgesia method was continuous epidural analgesia. 3) Age 18 years or older at the time of consent. 4) Written consent to participate in the study has been obtained from the patient.

Exclusion criteria

Exclusion criteria: 1)Extremely emergent cesarean section(We had no time for explanation). 2)Patients who have an allergy to morphine, fentanyl, or bupivacaine. 3)Anesthesia was changed due to inadequate anesthetic effect of spinl anesthesia.

Design outcomes

Primary

Measure	Time frame
Anesthesia satisfaction	—

Countries

Japan

Contacts

Public ContactShuji Uchimura

National Hospital Organization Miyakonojo Medical Center Department of Anesthesiology

syuji_uchimura@med.miyazaki-u.ac.jp0986-23-4111

Outcome results