Investigation of the optimum rate of patient controlled epidural analgesia after cesarean section

Investigation of the optimum rate of patient controlled epidural analgesia after cesarean section - Investigation of the optimum rate of patient controlled epidural analgesia after cesarean section

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000009939

Enrollment

Registered

2013-04-01

Start date

2013-04-01

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

Rate of the patient controlled epidural analgesia

2ml/h Rate of the patient controlled epidural analgesia

4ml/h Rate of the patient controlled epidural analgesia

6ml/h

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Parturients : age 20 to 50 and ASA physical status I and II

Exclusion criteria

Exclusion criteria: Ptient refusal; known fetal anomalies; contraindication for combined spinal-epidural anesthesia because of hemodynamic, infectious, hemostatic, or neurological problems; severe preeclampsia; contraindication for the drugs used in the protocol; or failure of combined spinal-epidural anesthesia

Design outcomes

Primary

Measure	Time frame
Degree of postcesarean analgesia	—

Countries

Japan

Contacts

Public ContactIKUOMI MIKUNI

Asahikawa Medical University Department of Anesthesiology and Critical Care Medicine

mikuni-ikuomi@kbd.biglobe.ne.jp0166-68-2583

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026