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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03790969
Other study ID # JEP-2018-654
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 15, 2019
Est. completion date December 31, 2019

Study information

Verified date March 2019
Source National University of Malaysia
Contact Chuah Sion Keat
Phone +617-3818580
Email cskeat@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To study the pain experience of trigger finger steroid injection with 26 gauge needle as compared to 23 gauge needle.


Description:

compare pain experience of trigger finger steroid injection between 26 gauge needle and 23 gauge needle.


Recruitment information / eligibility

Status Recruiting
Enrollment 112
Est. completion date December 31, 2019
Est. primary completion date November 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age above 18 year old

- Male or female(non-pregnant)

- Single trigger finger

- Clinically diagnosed trigger finger- Green classification Grade I or II

- No prior surgery to the involved finger

- Subject is able to provide voluntary, written informed consent

Exclusion Criteria:

- Age less than 18 year old

- Allergy to lignocaine or corticosteroid

- Trigger finger with Green classification grade III or IV

- Previous surgery on the affected finger

- Any wound, neurovascular injury, or skin disease at injection site

- Concomitant ipsilateral fingers/wrist/forearm/arm injury

- Preexisting congenital/acquired deformities of hand (such as rheumatoid arthritis, contracture)

- Insensate hand

Study Design


Related Conditions & MeSH terms


Intervention

Device:
26 gauge needle
smaller gauge needle
23 gauge needle
control group

Locations

Country Name City State
Malaysia Chuah Sion Keat Cheras Kuala Lumpur

Sponsors (1)

Lead Sponsor Collaborator
National University of Malaysia

Country where clinical trial is conducted

Malaysia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual analog scale-pain A numerical rating scale of 0 to 100, with 0 meaning no pain and 100 meaning the worst pain one minute after injection
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