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Ultrasound guided by ESPB and TAPB used in patients with abdominal radical hysterectomy the efficacy and safety of postoperative analgesia: a double-blind, randomized, controlled study

Ultrasound guided by ESPB and TAPB used in patients with abdominal radical hysterectomy the efficacy and safety of postoperative analgesia: a double-blind, randomized, controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044240
Enrollment
Unknown
Registered
2021-03-12
Start date
2021-03-15
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Abdominal radical hysterectomy

Interventions

TAPB Group:TAPB combined with PCIA
ESPB Group:ESPB combined with PCIA

Sponsors

The First Affiliated Hospital of USTC Anhui Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years; 2. To plan abdominal radical hysterectomy and require patients postoperative analgesia; 3. ASA physical fitness level I-II; 4. Patients without communication disorders. Patients can cooperate interventions on the use of implementation and understanding of relevant inventory, can operation patient controlled analgesia device; 5. Subjects were informed, voluntary and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with nerve block contraindications(e.g.puncture infection); 2. Patients with serious disease of the liver and kidney disease, blood system diseases (e.g.blood coagulation dysfunction); 3. Patients with a previous history of abdominal surgery or trauma; 4. Patients with the long-term use of sedation analgesia drugs or alcohol, calm analgesic drug addicts; 5. Chronic pain; 6. Used in the study of drug allergy; 7. Patients with evaluation of perception and pain of mental illness; 8. Patients with preoperative drugs; 9. Patients with pregnancy or lactation women; 10. Patients with diffuse peritonitis, umbilical hernia, diaphragmatic hernia, abdominal wall hernia, inguinal hernia, or femoral hernia; 11. Patients within 30 d or participated in other clinical research; 12. The researchers think that unsuitable to participate in the research of other conditions.

Design outcomes

Primary

MeasureTime frame
postoperative VAS pain score;Ramsay sedation scale score;the first request time for PCIA bolus;

Secondary

MeasureTime frame
postoperative opioid administered;dosageof postoperative rescue drugs;The occurrence of postoperative adverse reactions;postoperative recovery;

Countries

China

Contacts

Public ContactZhou Ling

The First Affiliated Hospital of USTC Anhui Provincial Hospital

13866702756@163.com+86 13866702756

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026