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An experiment to compare the efficency of laser and medicine (pregbalin) in recovery of nerve deficits in patients undergoing operation for maxillofacial trauma.

Phase 4
Conditions
Health Condition 1: G978- Other intraoperative and postprocedural complications and disorders of nervous system
Registration Number
CTRI/2019/11/021981
Lead Sponsor
MGM Dental College and Hospital Navi Mumbai
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) Participants of both the genders between age group of 18-60 years.

2) Participants with post traumatic neurosensory disturbances of infraorbital or inferior alveolar nerves in unilateral facial fractures requiring open reduction and internal fixation.

3) Participants willing for the study and follow up.

Exclusion Criteria

1) Isolated zygomatic arch and condylar process fractures.

2) Participants with neurologic disorder like seizures.

3) Participants with systemic diseases such as diabetes, Thyroid disorders, carcinomas, on steroids etc.

4) Pregnant females.

5) Participants with a history of head injury, Uncooperative and mentally retarded participants.

6) Isolated soft tissue lacerations and avulsion injuries

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Compare the effectiveness of low level diode laser therapy(LLLT) and conventional medical therapy using two point discrimination , pin prick stimuli and thermal discrimination conducted on various intervals upto 6 months for recovery of infraorbital or inferior alveolar neurosensory deficits.Timepoint: 24 hours prior to surgery, 48hrs after surgery, 7th day, after 1 month, 3 months and 6 months.
Secondary Outcome Measures
NameTimeMethod
1) Degree of neurosensory deficit of infraorbital and inferior alveolar nerve. <br/ ><br>2) Progress of recovery of neurosensory deficit of infraorbital and inferior alveolar nerve. <br/ ><br>Timepoint: 24 hours prior to surgery, 48hrs after surgery, 7th day, after 1 month, 3 months and 6 months.
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