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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04610307
Other study ID # CMHLahore
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 1, 2020
Est. completion date December 1, 2020

Study information

Verified date October 2020
Source Combined Military Hospital, Pakistan
Contact Anum Arif
Phone +923422398424
Email dranumarif@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pain and satisfaction score will be assessed at the end of surgery and compared in either of two groups


Description:

All patients meeting inclusion criteria will be randomly enrolled in two groups. Intervention group will receive buffered lignocaine . at the end of procedure data will be recorded regarding pain VASscore and satisfaction score


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date December 1, 2020
Est. primary completion date December 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - ASA I to III - Brachiocephalic arteriovenous fistula - Radiocephalic arteriovenous fistula Exclusion Criteria: - basiic vein transposition - redo surgery emergency surgery - failure to understand the questionnnare

Study Design


Intervention

Procedure:
buffered anesthesia
patients will undergo surgery under buffered local anesthesia

Locations

Country Name City State
Pakistan Combined Military Hospital Lahore

Sponsors (1)

Lead Sponsor Collaborator
Combined Military Hospital, Pakistan

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary pain score pain score on visual analog score on a scale of 0 to 10. 0 means no pain. 1 is least pain and 10 is maximum pain 60 minutes
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