Assessing Pain Relief in Dental Implant Surgery: Comparing Two Laser Therapies

Phase 2

Not yet recruiting

• Conditions: Health Condition 1: K068- Other specified disorders of gingiva and edentulous alveolar ridge

• Registration Number: CTRI/2024/05/066673
• Lead Sponsor: Dr Pankaj Dhawan

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 27 May 2024

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Patients shall be chosen without regard to their financial situation, gender, caste, or religion.

2. A patient in generally good health.

3. Individuals with less than a 20% visible plaque index who practice adequate oral hygiene.

4. Availability of bone for implant insertion, with minimum thickness and height of 10 mm;

5. Loss of posterior teeth on either sides of the jaw; and

6. Adequate interocclusal height to modify the surgical guide prototype and execute the osteotomies

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
PAIN PERCEPTION ASSESSMENTTimepoint: pre operatively, after 24hrs and after 36hrs post operatively

Secondary Outcome Measures

Name	Time	Method
ATimepoint: NA