The analgesic effect of ultrasound-guided transversus abdominis plane block combined with transversalis fascia plane block in elective caesarean section

The analgesic effect of ultrasound-guided transversus abdominis plane block combined with transversalis fascia plane block in elective caesarean section: a prospective, randomized, controlled clinical trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900025884

Enrollment

Unknown

Registered

2019-09-12

Start date

2019-09-10

Completion date

Unknown

Last updated

2019-09-16

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

Conditions

postoperative pain

Interventions

experimental group:TAP+TEP

control group:Intravenous analgesia

Eligibility

Sex/Gender

Female

Age

18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Aged 18 to 35 years, pregnant women for elective caesarean section.

Exclusion criteria

Exclusion criteria: 1. refused to participation; 2. long-term(more than 3 months) adminstered with analgesic or opioid dependent. 3. dementia, language barrier or other reasons causing unable to communicate; 4. allergy to the local anesthetic; 5. infection of the puncture site or severe coagulation dysfunction; 6. considered unsuitable to enrollment by investigator.

Design outcomes

Primary

Measure	Time frame
consumption of opioid medicine during the first 24h postoperative;	—

Secondary

Measure	Time frame
postoperative pain score;PONV;time of loss-of-sensation for the spinal anesthesia;time of first rescue analgesia;length of stay-in hospital;	—

Countries

China

Contacts

Public ContactBingliang Sun

Peking University First Hospital

838992892@qq.com+86 0315-5157269

Outcome results

None listed

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