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Comparation of the efficacy and onset of the distribution circumferencial va not ircumferencial of local anesthetic in the median and ulnar nerves for surgery of carpal tunnel

Comparation of the efficacy and onset of the distribution circumferencial va not ircumferencial of local anesthetic in the median and ulnar nerves for surgery of carpal tunnel - ArAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2011-002608-34-ES
Enrollment
Unknown
Registered
2011-10-03
Start date
2011-11-21
Completion date
Unknown
Last updated
2015-10-12

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

Conditions

Sheduled patients for surgery of carpal tunnel MedDRA version: 14.0 Level: PT Classification code 10007695 Term: Carpal tunnel decompression System Organ Class: 10042613 - Surgical and medical procedures

Interventions

Trade Name: Mepivacaina Braun ampolla 10 ml 1% Product Name: MEPIVACAÍNA Pharmaceutical Form: Solution for injection INN or Proposed INN: MEPIVACAINA HIDROCLORURO CAS Number: 1722-62-9 Other descripti

Sponsors

Paula Diéguez García
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Sheduled patinets for surgery of carpal tunnel incluyed all patient clasification ASA I-III, without exclusion criterios and read and undestand and firm informed consent Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 90 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 34

Exclusion criteria

Exclusion criteria: Anormal bleeding, infection in the punction side, alergy or other problems with the medication of the study, muscular or nerve diseases, patients < 18 years old, pregnancy, cognitive disease or reject of the patient

Design outcomes

Primary

MeasureTime frame
Main Objective: The main objective of the clinical trial is the evaluation of the efficacy and onset of the distribution circumferencial vs no circumferencial of the local anesthetic around the median and ulnar nerves in sheduled patients for surgery of the carpal tunnel syndrom;Secondary Objective: The secundary objetives are: evaluation of the demography characteristics of the population, the postoperative time and spread local anesthetic around the median and ulnar nerves;Primary end point(s): The main variables are efficacy and onset of the median and ulnar block. The efficacy will detected with cold sensitivity, with cold cotton, on the fingers of blocked arm. The onset will detected with the exploration of sensitivity at 5, 15, 30 minutes after block nerve and at threat to Postoperative Room.;Timepoint(s) of evaluation of this end point: In the Postoperative room—

Secondary

MeasureTime frame
Secondary end point(s): The postoperative time and spread local anesthetic around the median and ulnar nerves;Timepoint(s) of evaluation of this end point: 24 hours postoperative—

Countries

Spain

Contacts

Public ContactPaula

Paula Diéguez García

pauladieguez@yahoo.com687995525

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 18, 2026