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Comparing the Position of Collagen Membrane During Immediate Implant Placement

Compraing the Effect of Placement of Collagen Membrane Inside the Extraction Socket and Outside it During Immediate Implant Placement

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04224935
Enrollment
20
Registered
2020-01-13
Start date
2018-12-01
Completion date
2020-01-01
Last updated
2026-02-18

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

Conditions

Badly Decayed Teeth, Immediate Dental Implant Placement, Immediate Implant Placement

Keywords

immediate implant placement, badly decayed tooth in esthetic zone, collagen membrane, xenograft, temporization

Brief summary

evaluation of the use of collagen membrane inside the socket and outside it during immediate implant placement

Detailed description

Twenty patients, who are candidates for immediate implant placement, will participate in this prospective clinical trial. Group 1(10 patients) : immediate implant placement with bone graft and collagen memebrane outside the buccal plate Group 2 (Control group)(10 patients) : immediate implant placement with bone graft and collagen memebrane inside the buccal plate assessment of the buccal bone thickness assessment of soft tissue thickness • Esthetic outcome evaluation Will be done using the root coverage esthetic score (Cairo et al. 2009) that include Both evaluations will be done at 3, 6 and 9 months

Interventions

PROCEDURECollagen membrane inside

during immediate implant placement the collagen membrane will be placed in the jumping gap

PROCEDURECollagen membrane outside

during immediate implant placement the collagen membarne will be placed on the surface of the buccal plate of bone

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Systemically free patients (American Society of Anesthesiologists I; ASA I). * Age range (20 -50) years. * Good compliance with the plaque control instructions following initial therapy. * Patients diagnosed badly decayed tooth in esthetic zone indicated for immediate implant placement * Availability for follow up and maintenance program.

Exclusion criteria

* Patient suffering from periodontitis * Presence of smoking habit. * Presence of occlusion interference. * Pregnant and lactating females. * Vulnerable group of patients (handicapped, mentally retarded and prisoners).

Design outcomes

Primary

MeasureTime frameDescription
buccal plate of bone thicknessbaseline 12 monthsassessment of the buccal plate of bone will be determined in mm from CBCT

Secondary

MeasureTime frameDescription
soft tissue thickness (Volumetric assessment)baseline, 6 and 12 monthsPreoperative scanning will be done. At 6,12 months after surgical procedure the same procedure will be done to determine the soft tissue thickness after the surgery. The difference between the tissue thickness before and after

Countries

Egypt

Contacts

STUDY_CHAIRMai Shafik, professor

Misr international univeristy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026