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Noval technique in management of condylar fracture with irrigation of jaw joint.

EFFICACY OF ARTHROCENTESIS WITH HEMATOMA BLOCK AND CLOSED REDUCTION FOR MANAGEMENT OF CONDYLAR FRACTURES ASSOCIATED WITH OR WITHOUT OTHER MANDIBULAR FRACTURES-A RANDOMIZED CLINICAL TRIAL.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021432
Enrollment
36
Registered
2019-09-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: S026- Fracture of mandible

Interventions

Intervention1: ringers lactate solution (Aculife): Arthocentesis in experimental group with ringers lactate solution. ringer�s lactate solution into the temporomandibular joint cavity (JC) of

Sponsors

Government dental college and hospital Mumbai
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients willing to participate in study. 2. Patients with condylar fractures with or without other mandibular fractures. 3. Patients reporting OPD within 1 week after injury. 4. Patients with condylar fracture of type 1 and type 2 according to Wassmundââ?¬•s classification and according to MacLennan classification a)no displacement, and b)deviation 5. Patients with intracapsular and condylar neck fracture . 6. Patients willing for closed reduction.

Exclusion criteria

Exclusion criteria: 1) Patients without condylar fractures. 2) Patients reporting to OPD after 1 week of injury. 3) Patients willing for open reduction and internal fixation. 4) Patients with communited/displaced condylar fracture. 5) Patients with history of any TMJ disorder or any invasive procedure on TMJ. 6) Patients having history of any systemic diseases. 7) Patients with history of asthma, epilepsy etc. where intermaxillary fixation are contraindicated. 8) Pregnant and lactating patient. 9) Patients which are unable to follow study protocol. 10) A patient with any other associated Cranio-maxillary fractures except mentioned in inclusion criteria.

Design outcomes

Primary

MeasureTime frame
1) Evacuation of hematoma 2) Immediate pain in TMJ region during reduction of fracture will be assessed on VAS scale. 3) Postoperative anatomical reduction condylar fracture on CBCT. 4) Postoperative pain in TMJ on VAS scale on 3 weeks, 3 and 6 months of intervals.Timepoint: 1) immediately during reduction of fracture 2) Immediate 3) immediate 4) at 3 weeks, 3 and 6 months of intervals.

Secondary

MeasureTime frame
Range of motion will be measured by tongue blade technique at interval of preoperatively, 3 weeks postoperatively, 3 and 6 months on follow up.Timepoint: preoperatively, 3 weeks postoperatively, 3 and 6 months on follow up.

Countries

India

Contacts

Public ContactMaroti Baburao Wadewale

Government dental college and hospital Mumbai

prajwalitkende1979@gmail.com09324715824

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026