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临床试验/CTRI/2025/02/081404
CTRI/2025/02/081404尚未招募3 期

Clinical and Radiographic Assessment of Apical Periodontitis with Calcium Hydroxide vs Triple Antibiotic Paste Both when used along with Chlorhexidine Digluconate as Vehicle : A Randomized Controlled Trial

Dr Harnoor1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年3月10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
50
试验地点
1
主要终点
The primary objective will focus on

研究概览

简要总结

Patients will be randomly assigned to two groups:

• Group A: Calcium Hydroxide + 2% Chlorhexidine Digluconate

• Group B: Triple Antibiotic Paste + 2% Chlorhexidine Digluconate

Procedure:

• Patients will undergo endodontic treatment with intracanal medicaments.

• Standard protocol will be followed, including anesthesia (2% lignocaine with 1:80,000 adrenaline), rubber dam isolation, caries excavation, access opening, and root canal preparation using Ni-Ti rotary files.

• Canals will be irrigated with sodium hypochlorite, normal saline, and 17% EDTA, then dried with sterile paper points.

Intracanal Medication Protocol:

• Step I: Intracanal medicament applied, changed after 7 days.

• Step II: Medication retained for another 7 days.

• After 15 days, the master cone will be selected, and the canals will be obturated.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • Adult Patients aged between 18 and 45 years.
  • Single-rooted teeth (anterior and posterior).
  • Teeth with Apical periodontitis.
  • Teeth with necrotic pulp that gave a negative response to vitality testing.

排除标准

  • Non-restorable teeth.
  • Teeth requiring retreatment.
  • Teeth with calcified canals.
  • Teeth with internal/external root resorption.
  • Patients with serious medical illness.
  • Patients with known allergies to the materials used in the study.

结局指标

主要结局

The primary objective will focus on

时间窗: at the interval of 1 month, 3 months and 6 months

periapical healing

时间窗: at the interval of 1 month, 3 months and 6 months

次要结局

  • Postoperative pain will be assessed as a secondary(outcome.)

研究者

发起方
Dr Harnoor
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Harnoor

Deaprtment of Conservative Dentistry and Endodontics Himachal Dental College Sundernagar

研究点 (1)

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