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The Effect of Ultrasound Guided Transversus Abdominis Plane Block Analgesia after Cerean Section

The Effect of Ultrasound Guided Transversus Abdominis Plane Block Analgesia after Cerean Section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15007077
Enrollment
Unknown
Registered
2015-09-14
Start date
2015-09-14
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

caerean section

Interventions

A:Injecting 20ml of 0.35% ropivacaine the transversus abdominis plane
B:Injecting 15ml of 0.35% ropivacaine transversus abdominis plane, 5ml internal oblique
C:Injecting 10ml of 0.35% ropivacaine transversus abdominis plane, 10ml internal oblique
D:Injecting 5ml of 0.35% ropivacaine transversus abdominis plane, 15ml internal oblique

Sponsors

The First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: The patients of cerean section, ASA I or II, QTc interval analysis of ECG before operation, QTc<0.47, agreeing that ultrasound guided transversus abdominis plane block is used for multimodal analgesia after cerean section.

Exclusion criteria

Exclusion criteria: Patients are excluded if they are or have: 1. allergic to local anesthetic; 2. abnormal coagulation function; 3. abnormal liver kidney function; 4. history of nerve or muscle abnormalities; 5. history of abdominal surgery or radiotherapy; 6. skin damage infection of abdominal wall; 7. mental illness; 8. unable to understor to express VAS pain scores correctly; 9. taking drugs that affect CYP1A2 metabolism of ROP (eg, fluvoxamine); 10. taking drugs that may prolong QTc interval (eg, haloperidol, amiodarone, sotalol).

Design outcomes

Primary

MeasureTime frame
VAS;morphine consumption;the plasma ropivacaine concentrations of 15min, 30min, 2h, 4h after operation;

Secondary

MeasureTime frame
presence severity of PONV Sedation at 2h, 4h, 8h, 12h, 24h;

Countries

China

Contacts

Public ContactQun Lin
wangjing83429450@163.com+86 13859091369

Outcome results

None listed

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