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The effects of ultrasound-guided bilateral rectus sheath block (RSB) in Laparo Endoscopic Single-Site Surgery (LESS) of day-gynecology, a randomized controlled study

The effects of ultrasound-guided bilateral rectus sheath block (RSB) in Laparo Endoscopic Single-Site Surgery (LESS) of day-gynecology, a randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042433
Enrollment
Unknown
Registered
2021-01-21
Start date
2021-02-08
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Day-gynecological LESS

Interventions

Oral ibuprofen:Oral 10ml ibuprofen after the operation and NRS scores more than 3
Local anesthesia:when the operation ends, the operatior fulfil the LA with 0.33% ropivacaine to umbilical incision
ultrasound-guided bilateral rectus sheath block (RSB):When operation ends,the same senior anesthesiologist fulfil the Ultrasound guided bilateral RSB with 15ml 0.33%ropivacaine.

Sponsors

Chengdu Women's and Children's Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years; 2. Undergoing day-gynecological LESS; 3. ASA degree: I-II.

Exclusion criteria

Exclusion criteria: 1. Combined with serious complication of cardiac\brain\renal\liver; 2. Be allergy to ropivacaine or ibuprofen; 3. Have long term usage of analgesics; 4. Be psychological disorder; 5. Had an operation before.

Design outcomes

Primary

MeasureTime frame
The NRS scores;Usage of ibuprofen (time of administration\tota dosage);patient satisfaction;

Secondary

MeasureTime frame
Time to get up after operation;Time to urinate, exhaust after operation;The incidence rate of PONV;The incidence rate of shoulder pain;

Countries

China

Contacts

Public ContactKe Huang

Chengdu Women's and Children's Central Hospital

626909686@qq.com+86 13438204740

Outcome results

None listed

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