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Assessment of implant retention and alteration of the gums in early/ late implant placement among smokers

Evaluation Of Secondary Stability And Soft tissue Variation Following Immediate And Late Implant Placement Among Smokers - An Observational Study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058645
Enrollment
40
Registered
2023-10-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Z915- Personal history of self-harm

Interventions

Intervention1: Test group: Late Implant placement in smokers (Group III) Intervention2: Test group: Immediate Implant placement in Smokers (Group IV) Control Intervention1: control group: Late impla

Sponsors

Poorani A E
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria for Smoker individuals:1. patients with Healed Ridge(6 months of extraction postoperatively) [Group I and Group III]2. patients with Fresh Extracted Socket [Group II and group IV].3. Non Smoker patients that include who have never smoked [Group I and group II].4. Patients who are between 25-60 years of age.5. Smoker patients that include who have smoke morethan 10 cigrattes per day [Group III and group IV].Inclusion criteria for Non Smoker individuals:1. patients with Healed Ridge(6 months of extraction postoperatively) [Group I and Group III].2. patients with Fresh Extracted Socket [Group II and group IV].3. Non Smoker patients that include who have never smoked [Group I and group II].

Exclusion criteria

Exclusion criteria: Exclusion criteria for Smoker individuals: 1. History of oral /intravenous bisphosphonate use for >3 years. 2. Pregnancy or lactation 3. Known allergy to any material or medication used in the study. 4. Any Previous History of head and neck radiation therapy 5. Chemotherapy in the last 12 months 6. Severe psychologic problems 7. Patient not willing to sign the consent approved by the Human Studies Committee. Exclusion criteria for Non smoker individuals: 1. Smokers. 2. History of oral /intravenous bisphosphonate use for >3 years 3. Pregnancy or lactation 4. Known allergy to any material or medication used in the study. 5. Any Previous History of head and neck radiation therapy 6. Chemotherapy in the last 12 months 7. Severe psychologic problems 8. Patient not willing to sign the consent approved by the Human Studies Committee.

Design outcomes

Primary

MeasureTime frame
To evaluate the secondary stability using resonance frequency analyser and crestal bone levels in the Non Smoker and Smoker individuals Timepoint: Baseline 4 week 8 week 12 week 16 week

Secondary

MeasureTime frame
To assess the papillary height,pink esthetic score,assessment of pain and wound healing index in Non smokers and smokers individuals. Timepoint: Baseline 4 week 8 week 12 week 16 week;To evaluate the primary stability using Resonance Frequency Analyser in smoker and non smokers individuals. Timepoint: Baseline

Countries

India

Contacts

Public ContactDr Harinath Parthasarathy

SRM DENTAL COLLEGE

harinatp@srmist.edu.in9840482400

Outcome results

None listed

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