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Comparison of Two Types of Pain Relief After Cesarean Delivery

Comparison of Two Methods of Pain Relief After Cesarean Delivery: Transversus Abdominis Plane (TAP) Block Versus Incisional Infiltration With Local Anesthetic

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01151943
Acronym
Cesar-Dol
Enrollment
77
Registered
2010-06-29
Start date
2010-10-31
Completion date
2012-07-31
Last updated
2016-11-03

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

Conditions

Cesarean Section

Keywords

cesarean section, continuous wound infiltration, transversus abdominis plane block

Brief summary

Women undergoing elective cesarean delivery, performed under a standard spinal anesthesia, will be randomized to undergo either TAP block or incisional infiltration with local anesthetic, in addition to standard postoperative analgesia comprising regular acetaminophen, nefopam and ketoprofen. Short acting oral morphine will be given as a rescue treatment in case of severe pain.

Interventions

OTHERTransversus Abdominis Plane (TAP) Block

Bilateral injection of levobupivacaine (20 mL, 3.75 mg/mL)

OTHERIncisional Infiltration of Local Anesthetic

continuous administration of levobupivacaine (1,25 mg/mL,5 mL/h) during 48 hours.

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* scheduled cesarean section performed under spinal anesthesia * ASA I or II * height above 1,55 m * singleton pregnancy

Exclusion criteria

* contre indication to a drug used in the study (levobupivacaine, ketoprofen, nefopam)

Design outcomes

Primary

MeasureTime frame
severity of postoperative pain48 postoperative hours

Secondary

MeasureTime frame
morphine requirement48 postoperative hours
complication of each loco-regional techniqueend of hospitalisation
delay before the first rescue dose of morphine48 postoperative hours
length of hospital stayend of hospitalisation
occurrence of a neuropathic postoperative pain1 month postoperatively
patient's satisfactionend of hospitalisation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026