Minimizing Pain Experience In Trigger Finger Steroid Injection.
NCT ID: NCT03790969
Last Updated: 2019-03-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
112 participants
INTERVENTIONAL
2019-01-15
2019-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
A Trial Comparing Pain During Local Tumesent Injection In Fingers Using Different Syringe-Needle Combinations
NCT03736915
Two Different Tactile Stimulus Methods
NCT04594083
Ultrasound Needle Transducer for Regional Anesthesia Validation Study
NCT04726930
Comparison of Intravascular Uptake and Pain Perception During Epidural Injection Using 22 Gauge vs 25 Gauge Needle
NCT04350307
Intraoperative Cryoanalgesia for Extended Pain Management Following Thoracotomy
NCT03538340
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
26 gauge needle
intervention group
26 gauge needle
smaller gauge needle
23 gauge needle
control group
23 gauge needle
control group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
26 gauge needle
smaller gauge needle
23 gauge needle
control group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National University of Malaysia
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
CHUAH SION KEAT
medical officer
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Chuah Sion Keat
Role: PRINCIPAL_INVESTIGATOR
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Chuah Sion Keat
Cheras, Kuala Lumpur, Malaysia
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
JEP-2018-654
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.