Composite Plug Vs D-PTFE Membrane in Socket Preservation
Recruiting
N/AInterventional Study
Alveolar Bone Loss
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
20 – 70
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
Cairo University · Other
Who this trial is looking for
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The aim of the current study is to compare the effect socket sealing with flowable resin composite compared to dense polytetrafluoroethylene membrane after filling the extraction site with xenograft particles in terms of soft and hard tissue changes, procedural time, post operative pain, patients' satisfaction, and cost effectiveness.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients having single non-adjacent hopeless maxillary tooth in the esthetic zone that are indicated for extraction.
* Patients with healthy systemic condition.
* Patients aged from 20 to 70 years old.
* Good oral hygiene.
* Accepts 4 months follow-up period (cooperative patie…
Inclusion Criteria:
* Patients having single non-adjacent hopeless maxillary tooth in the esthetic zone that are indicated for extraction.
* Patients with healthy systemic condition.
* Patients aged from 20 to 70 years old.
* Good oral hygiene.
* Accepts 4 months follow-up period (cooperative patients).
Exclusion Criteria:
* Systemic diseases or medications that might affect bone metabolism, increase surgical risk or complicate post-operative healing.
* Previous bone augmentation to implant site.
* Untreated periodontal diseases.
* Para-functional habits such as bruxism and clenching.
* History of radiation therapy to the head and neck.
* Heavy smokers (≥ 10 cigarettes per day).
* Pregnant or lactating females.
* Alcoholism or drug abuse.
* Psychiatric problems.
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