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Facial Gingival Level Evaluation Following Soft Tissue Augmentation Using CTG Around Immediate Dental Implants vs Immediate Dental Implants Alone in the Esthetic Zone.

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Immediate Dental Implants Connective Tissue Graft Esthetic Zone

Treatments

Procedure: Intervention group:(Group B) connective tissue graft combined with immediate implant.

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Aim of current study to evaluate connective tissue graft combined with immediate implant placement as an innovative option for less facial gingival tissue recession, less pocket depth and less clinical attachment loss versus immediate implant alone.

Full description

P: Adult patients with single or multiple non-restorable teeth in esthetic zone I: Immediate implant + Connective tissue graft. C: Immediate implant alone. O: Primary Outcome: Facial gingival level Secondary Outcome: Patient satisfaction, probing depth, probing attachment loss, tissue biotype, keratinized mucosal width and bleeding on probing.

P.M will select patients from the outpatient clinic of the Oral Medicine and Periodontology Department - Cairo University. Screening of patients will continue until the target population is achieved. Identifying and recruiting potential subjects is achieved through patient database.

Enrollment

18 patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 18-55
  2. Patients with single or multiple non-restorable teeth in maxillary anterior or premolar area.
  3. Patients with adequate bone volume for the dental implant procedure.
  4. Patients who are compliant to oral hygiene measures.
  5. Patient consent approval and signing.

Exclusion criteria

  1. Heavy smokers.
  2. Systemic disease that contraindicates implant placement or surgical procedures.
  3. No or poor patient's compliance.
  4. Psychological problems.
  5. Pathology at the site of intervention.
  6. Pregnancy females.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

18 participants in 2 patient groups

Control group: immediate implant alone
Active Comparator group
Description:
Patient will be treated with immediate implant alone.
Treatment:
Procedure: Intervention group:(Group B) connective tissue graft combined with immediate implant.
(Group A) immediate implant alone
Active Comparator group
Description:
Patient will be treated with immediate implant alone.
Treatment:
Procedure: Intervention group:(Group B) connective tissue graft combined with immediate implant.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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