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To Assess The Lower Jaw Fracture Site Bone Density After Using Calcitonin Hormone Spray

Evaluation of the efficacy of salmon calcitonin nasal spray on bone density in the treatment of mandibular fractures-a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/048738
Enrollment
12
Registered
2023-01-04
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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: Calcitonin Nasal Spray: Salmon Calcitonin Nasal Spray 200 IU (1 puff daily) for 30 days Control Intervention1: No nasal spray: No placebo is given

Sponsors

Dr Firdous Abdul Sathar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with isolated mandibular fracture involving symphysis, parasymphysis, body, or angle 2. The age range of 18-50 years 3. Patients categorized as ASA I Status 4. Patients tolerant to the calcitonin nasal spray

Exclusion criteria

Exclusion criteria: 1. Comminuted mandibular fractures 2. Patients with any bony pathologies or thyroid dysfunctions 3. Individuals categorized under ASA II, III, or IV 4. Patients who have negative surgical outcomes such as postoperative malocclusion, interfragmentary mobility, or step deformity

Design outcomes

Primary

MeasureTime frame
1. To evaluate the efficacy of salmon calcitonin on postoperative pain in mandibular fracture patients. 2. To assess the change in levels of plasma osteocalcin after administration of salmon calcitonin. 3. To evaluate the bone density following open reduction and internal fixation of mandibular fractures after administration of salmon calcitonin. Timepoint: 1.Visual Analogue Scale on 1st,3rd, and 5th post-operative days. 2. Serum osteocalcin levels before surgery and after 4 weeks. 3. Density of bone at fracture site by CBCT scans taken at 2 weeks and 4 weeks postoperatively.

Secondary

MeasureTime frame
To assess a better quality of life in these patients by fore said parameters.Timepoint: Follow up for 1 month.

Countries

India

Contacts

Public ContactDr Firdous Abdul Sathar

YENEPOYA DENTAL COLLEGE, MANGALORE, KARNATAKA

arvind_raoht@rediffmail.com9448142508

Outcome results

None listed

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