L-PRF vs Connective Tissue With Customized Healing Abutment in Immediate Implant Placement
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: L-PRF with dental implant and customized healing abutment, Connective tissue with dental implant and customized healing abutment.
- Who it may be relevant to
- Registry conditions: Recession, Gingival, Bone Loss in Jaw. Basic parameters: 21 years — 45 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Evaluation of Soft and Hard Tissue Augmentation by Connective Tissue Graft or Leukocyte-Platelet Rich Fibrin in Immediate Implant Placement With Customized Healing Abutment: A Randomized Controlled Clinical Trial.
Overview
comparison between L-prf and connective tissue with dental implant
Detailed description
comparison between L-PRF and Connective tissue with customized healing abutment regaring soft and hard tissue outcomes with immediate dental implants.
Interventions
- Procedure L-PRF with dental implant and customized healing abutment
L-PRF with dental implant and customized healing abutment - Procedure Connective tissue with dental implant and customized healing abutment
Connective tissue with dental implant and customized healing abutment
Primary outcome measures
- Patient-reported pain experience [Time frame: first 7 days after surgery]
- Pink aesthetic score [Time frame: before surgery, 3 months and 6 months after surgery]
- crestal bone loss [Time frame: preoperative and 6 months post operative]
Secondary outcome measures (3)
- Gingival thickness [Time frame: pre opearative, 3 and 6 months post operative]
- probing pocket depth [Time frame: preoperative , 3 and 6 months post operative]
- keratinized tissue width [Time frame: preoperative , 3 and 6 months post operative]
Eligibility criteria
Inclusion criteria
- Intact labial/buccal bone plate
- The presence of non-restorable single-rooted maxillary centrals, canines or premolars.
- Sufficient bone volume.
- Good oral hygiene.
- Nonsmokers.
- Sufficient bone width (≥ 1 mm) in the buccal plate of the remaining bone to place an implant confirmed by cone beam computer tomography (CBCT).
Exclusion criteria
- Insufficient bone volume.
- Active infection.
- Patients on chemotherapy or radiotherapy.
- Patients who have systemic disorders {uncontrolled diabetes mellitus, autoimmune disease, …etc},
- Pregnant patients,
- Patients with bone diseases
- Presence of periapical pathology.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Kafrelsheikh University — Kafr ash Shaykh
Identifiers
NCT: NCT07102758 · KFSIRB200-436