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Joint replacement in patients with fused jaws.

Outcome assessment of Concomitant total temporomandibular joint replacement and Orthognathic surgery using indigenous patient specific implants in TMJ Ankylosis, A Prospective Cohort Pilot Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047574
Enrollment
24
Registered
2022-11-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: M266- Temporomandibular joint disorders

Interventions

Intervention1: Concomitant total temporomandibular joint replacement and Orthognathic surgery: i. TMJ prosthesis is fabricated as per the CTOS- CASS Protocol (as mentioned in our plan of work section

Sponsors

Indian Council of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i. Patients with Temporomandibular ankylosis ii. Patients with re-ankylosis of Temporomandibular joint after a failed surgery iii. Age: 18 years to 45 years

Exclusion criteria

Exclusion criteria: i. Patients with pre-existing co-morbidities that defer long surgery and impairs healing viz uncontrolled diabetes, vascular diseases, bleeding disorders not willing for optimization. ii. Edentulism without pros- thetic restoration iii. Patient with successful ankylotic release with adequate mouth opening over 35mm.

Design outcomes

Primary

MeasureTime frame
Maximum Bite ForceTimepoint: 1 Month, 3 month, 6 month Post Operative

Secondary

MeasureTime frame
Body Mass Index: evaluation of body mass indexTimepoint: Preoperatively and postoperatively at 3 months, 6 month.;Incidence of complications like peri-implant joint infection, reankylosis, facial nerve paresis, mandibular nerve sensory deficit.Timepoint: 1 Month, 3 month, 6 month, 1 year;Maximum interincisal openingTimepoint: Preoperative, 1 Month, 3 month, 6 month.;Obstructive sleep Apnoea evaluation using STOP-BANG and Modified Berlin QuestionnaireTimepoint: Preoperative, 1 Month, 3 month, 6 month.;Polysomnographic evaluation if any signs of OSATimepoint: Preoperative, 1 Month, 3 month, 6 month.;Posterior airway volumetric analysis using CT scan/CBCTTimepoint: Preoperative, 1 Month, 3 month, 6 month.;Quality of life assessment with WHOQOL-BREF scaleTimepoint: Preoperative, 1 Month, 3 month, 6 month.

Countries

India

Contacts

Public ContactSanthosh Rao

All India Institute of Medical Sciences Raipur

santhosh@aiimsraipur.edu.in9981525599

Outcome results

None listed

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