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Cutaneous sensory block area, Regression of blocked dermatomes after bilateral oblique subcostal transversus abdominis plane block under ultrasound guidance

Cutaneous sensory block area, Regression of blocked dermatomes after bilateral oblique subcostal transversus abdominis plane block under ultrasound guidance

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-16009037
Enrollment
Unknown
Registered
2016-08-16
Start date
2016-08-10
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

transversus abdominis plane block

Interventions

group of experimental: bilateral oblique subcostal transversus abdominis plane block under ultrasound guidance

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Aged older than eighteen years, abdominal skin intact sensation.

Exclusion criteria

Exclusion criteria: With history of allergy to ropivacaine or other drugs used in this trial, communication obstacle in language, ASA classification =3, body mass index= 18 or =30kg/m2,spinal demormities, neuropathy, spinal cord disorders

Design outcomes

Primary

MeasureTime frame
distribution characteristic of abdominal cutaneous sensory block area;cutaneous sensory block area of anterior abdominal wall;percent area of anterior abdomen blocked;cutaneous sensory block area of mid-abdominen;percent area of mid-abdomen blocked;Percent area of lateral-abdomen blocked;regression of blocked dermatomes;local anesthetic intoxication;nausea;vomit;haematoma;—

Countries

China

Contacts

Public ContactXuzhong Xu

the First Affiliated Hospital of Wenzhou Medical University

xuzhong@263.net+86 13706657799

Outcome results

None listed

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