跳至主要内容
临床试验/CTRI/2025/09/094339
CTRI/2025/09/094339尚未招募3 期

Evaluation of the Efficacy of Intranasal Salmon Calcitonin on Bone Healing Following Surgical Removal of Impacted Mandibular Third Molars — A Randomized Controlled Clinical Trial

Harni N1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年9月20日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
A total of 100 patients will be randomly divided into two groups: Group I will receive intranasal salmon calcitonin along with standard postoperative care, while Group II will receive only standard care.

研究概览

简要总结

This randomized controlled study will evaluate the efficacy of salmon calcitonin nasal spray on bone healing and postoperative pain following surgical removal of impacted third molar. A total of 100 patients will be randomly divided into two groups : Group 1 will receive intranasal salmon calcitonin along with standard postoperative care, while group 2 will receive standard care. Post op pain will be assessed using Visual Analogue Scale VAS on day 1,7,14,21 and 30, and bone healing will be evaluated by radiographic assessment of bone density at extraction site immediately after surgery, at 4 weeks and 12 weeks.

研究设计

研究类型
Interventional

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • Patients with impacted mandibular third molar.
  • Pederson difficulty index score of 6 and above.
  • Patients in the age group between 18 to 40 years ASA-1 category.

排除标准

  • Patients with seafood alleregy Patients with Peri apical pathology ASA-2,3,4,5 and 6 CATEGORIES Patient with any previous history of cardiomyopathy Patient with any known history of Thyroid dysfunction.
  • Patient undergoing therapies with bisphosphonates and immunosuppressants.
  • Patient with any known history of osteoporosis or pathologic fractures.
  • Asthmatic patients.

结局指标

主要结局

A total of 100 patients will be randomly divided into two groups: Group I will receive intranasal salmon calcitonin along with standard postoperative care, while Group II will receive only standard care.

时间窗: Postoperative pain will be assessed using the Visual Analog Scale on days 1, 7, 14, 21, and 30.

次要结局

  • bone healing will be evaluated by radiographic assessment of bone density at the extraction site immediately after surgery.(Assessed at 4 weeks, and at 12 weeks.)

研究者

发起方
Harni N
申办方类型
Other [Dental College]
责任方
Principal Investigator
主要研究者

Harni N

Madha Dental College

研究点 (1)

Loading locations...

相似试验