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Comparison of the effect of ultrasound-guided sacral anesthesia with different drug volumes in anorectal day surgery: a randomizec controlled trial.

Comparison of the effect of ultrasound-guided sacral anesthesia with different drug volumes in anorectal day surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036125
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Anorectall disease

Interventions

Group A:Ultrasound sacral block 15ml drug
Group B:Ultrasound sacral block 20ml drug

Sponsors

Second Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients who intend to undergo day anorectal surgery meet the admission criteria for day surgery: 1. The patient's age is greater than or equal to 18 years old and less than or equal to 70 years old; 2. ASA classification I-II level; 3. Anesthesia consultation is required (plan to complete the operation under non-local anesthesia); 4. Normal cognitive function, no serious mental illness, and the ability to sign informed consent; 5. There are no serious abnormalities in laboratory indicators such as blood routine, blood coagulation routine, and blood biochemistry.

Exclusion criteria

Exclusion criteria: 1. The patient refused to undergo spinal anesthesia; 2. Infection of the puncture site and skin damage; 3. Combined with diseases of important organ functions; 4. A history of tethered cord syndrome, space occupation in the spinal canal, etc..

Design outcomes

Primary

MeasureTime frame
Success rate of sacral anesthesia;

Secondary

MeasureTime frame
The anesthesia plane after the patient's sacral canal anesthesia;Anesthesia level of the patient after surgery;The patient’s postoperative urination time and urinary retention;NRS pain score at 1 hour, 6 hours after operation and at discharge;

Countries

China

Contacts

Public ContactMin Yan
zryanmin@zju.edu.cn+86 13757118632

Outcome results

None listed

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