Healing comfort and bone health in dental implants conventional versus flapless approach

Phase 4

Not yet recruiting

Conditions: Chronic periodontitis,

Registration Number: CTRI/2025/05/087825

Lead Sponsor: Dr Sankha Subhra Roy

Brief Summary: The purpose of this study is to compare marginal bone loss and soft tissue changes around implant and pain analgesic and swelling assessments at baseline and 3 months. The null hypothesis is that there is no significant difference between the two treatment modalities.

Detailed Description: Not available

Recruitment & Eligibility

Status: Not Yet Recruiting

Sex: All

Target Recruitment: 20

Inclusion Criteria

Age should be above or equals to 18 years Patient with partially edentulous area with minimum 5mm bone width and 8 mm bone length in maxilla or mandible Systematically healthy male and female with co operative ones should be included.

Exclusion Criteria

Patients having any adverse habits like smiking alcohol consumption Pregnant or lactating woman Uncontrolled systemic disease Allergy or hypersensitivity to any product used Mental or physical disorder Patients on bisphosphonates any evidence of pathology or active diseases of the implant bed and atrophy requiring bone regeneration in both width and height were excluded from the study.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
A clinicoradiological evaluation of marginal bone loss tissue changes post operative patients compliance in implants placed with flapless versus conventional surgical technique	Baseline and 3 months

Secondary Outcome Measures

Name	Time	Method

Trial Locations

Locations (1): Maharishi markandeshwar college of dental sciences and research
🇮🇳
Ambala, HARYANA, India
Maharishi markandeshwar college of dental sciences and research
🇮🇳Ambala, HARYANA, India
Dr Sankha Subhra Roy
Principal investigator
09310693160
perioprecision23roy@gmail.com