NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000021846

Registered date:20/04/2016

The analgesic efficacy of scheduled intravenous acetaminophen in combination with fentanyl intravenous patient controlled analgesia after cesarean section

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedwomen schedulled for cesarean section
Date of first enrollment2016/04/20
Target sample size40
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Acetaminophen 1g DIV 3 times per day 1day normalsaline 100ml DIV 3 times per day 1day

Outcome(s)

Primary OutcomeVisual analogue scale at rest and during motion at 0,1,3,6,12 hour after surgery
Secondary OutcomeThe frequency of additional analgesics, The time to first need for additional analgesics, Adverse effects

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximum45years-old
GenderFemale
Include criteria
Exclude criteriaEmergency cases, Patients with coagulation disorder and liver dysfunction ASA>3

Related Information

Contact

public contact
Name Keiko Shimohata
Address 2-5-22 Nishimachi,Kounanku,Niigata,Niigata Japan
Telephone 025-382-3111
E-mail migraine12jp@gmail.com
Affiliation Kameda Daiichi hospital Department of Anesthesiology
scientific contact
Name Keiko Shimohata
Address 2-5-22 Nishimachi,Kounanku,Niigata,Niigata Japan
Telephone 025-382-3111
E-mail migraine12jp@gmail.com
Affiliation Kameda Daiichi hospital Department of Anesthesiology