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evaluation of use of 3% sodium tetradecyl sulphate and 25% dextrose in the treatment of temporomandibular joint hypermobilty

EVALUATION OF EFFICACY OF 3% SODIUM TETRADECYL SULPHATE AND 25% DEXTROSE IN THE TREATMENT OF TEMPOROMANDIBULAR JOINT HYPERMOBILITY -A DOUBLE BLINDED -RANDOMISED CLINICAL TRIAL - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056023
Enrollment
30
Registered
2023-08-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified Health Condition 2: M266- Temporomandibular joint disorders

Interventions

Intervention1: INTERVENTION - PROLOTHERAPY: 2ML OF 25% DEXTROSE AND 0.5ML 3%SODIUM TETRADECYL SULPHATE ONCE EVERY 4 WEEKS FOR 4 SESSIONS Control Intervention1: prolotherapy in tmj hypermobilty with 3%

Sponsors

Dr Pimple Subham
Lead Sponsor
Dr Phani Kumar K
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with functional temporomandibular joint disorders including Internal Derangement, Subluxation and Dislocation. 2. Patients who are willing to participate in the study and give their consent

Exclusion criteria

Exclusion criteria: 1. Subjects under Anticoagulation therapy 2. Subjects with a History of total TMJ replacement, 3. Subjects with a Prior TMJ prolotherapy in the past 6 months 4. Subjects with TMJ injection within the past 3 months 5. Patients with concomitant inflammatory or infectious disorders of the TMJ 6. Patients with Daily use of opioid medication 7. Patients with Allergy or intolerance to study injections or pain medications 8. Patients with Connective tissue disorders

Design outcomes

Primary

MeasureTime frame
EVALUATION OF EFFICACY OF 3% SODIUM TETRADECYL SULPHATE AND 25% DEXTROSE IN TREATMENT OF TEMPOROMANDIBULAR JOINT HYPERMOBILITYTimepoint: 18 MONTHS

Secondary

MeasureTime frame
to determine the better treatment intervention between 25% dextrose prolotherapy and 3% sodium tetradecyl sulphateTimepoint: 18 months

Countries

India

Contacts

Public ContactDr I Nagamalleswar Rao

Anil Neerukonda Institute Of Dental Sciences.

dr.phanikumarkuchimanchi@anesehs.org8096339404

Outcome results

None listed

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