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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03684356
Other study ID # CairoU12
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date February 22, 2019
Est. completion date December 2020

Study information

Verified date February 2020
Source Cairo University
Contact Mohamed A Abd El Moneium, Ass.lecturer
Phone 01224302609
Email matef1989@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to clinically and radiographically evaluate the dimensional changes of soft and hard peri-implant tissues around single immediate post-extraction implants in the esthetic zone.


Description:

to compare the efficacy of the socket shield technique in counteracting the dimensional changes of the soft and hard peri-implant tissues to filliing the buccal gap with xenograft.

- Population (P): Patients with single non-restorable tooth in the esthetic zone.

- Intervention (I): Immediate implant placement with socket shield technique.

- Comparator (C): Immediate implant placement and filling the buccal gap with xenograft.

- Primary Outcome (O): Pink Esthetic Score (PES) (Fürhauser et al., 2005).

- Time frame: 9 months (Chu et al., 2015).

- Study design: Randomized controlled clinical trial.


Recruitment information / eligibility

Status Recruiting
Enrollment 22
Est. completion date December 2020
Est. primary completion date December 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Patient's age was 18 years or older.

2. Non-restorable tooth in the upper inter-bicuspid area.

3. Adequate bone volume for the placement of immediate implant.

4. Following tooth extraction, there was an intact socket bony wall (type I extraction socket).

5. Primary stability of the implant was achieved at the time of the implant placement.

Exclusion Criteria:

1. Patients who reported tobacco use in the past 5 years.

2. Patients who had severe periodontal destruction at the site of implant placement.

3. The presence of any signs of acute infection in the surgical site or the adjacent two natural teeth.

4. Patients who had history of any systemic disease that precludes the placement of implants.

5. Any disease that might affect bone metabolism as osteoporosis.

6. Patients taking medications that might affect bone turn over as bisphosphonates.

7. Physically or mentally handicapped patients.

8. Pregnant females.

9. Teeth with vertical root fractures on the buccal aspect

10. Teeth with any other pathologies affecting the buccal part of the root, for example, external or internal resorptions.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
socket shield technique
immediate implant placement with buccal part of the root is retained
xenograft
immediate implant placement with filling the buccal gap with xenograft

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (5)

Bäumer D, Zuhr O, Rebele S, Hürzeler M. Socket Shield Technique for immediate implant placement - clinical, radiographic and volumetric data after 5 years. Clin Oral Implants Res. 2017 Nov;28(11):1450-1458. doi: 10.1111/clr.13012. Epub 2017 Mar 23. — View Citation

Bramanti E, Norcia A, Cicciù M, Matacena G, Cervino G, Troiano G, Zhurakivska K, Laino L. Postextraction Dental Implant in the Aesthetic Zone, Socket Shield Technique Versus Conventional Protocol. J Craniofac Surg. 2018 Jun;29(4):1037-1041. doi: 10.1097/SCS.0000000000004419. — View Citation

Mitsias ME, Siormpas KD, Kotsakis GA, Ganz SD, Mangano C, Iezzi G. The Root Membrane Technique: Human Histologic Evidence after Five Years of Function. Biomed Res Int. 2017;2017:7269467. doi: 10.1155/2017/7269467. Epub 2017 Nov 22. — View Citation

Siormpas KD, Mitsias ME, Kontsiotou-Siormpa E, Garber D, Kotsakis GA. Immediate implant placement in the esthetic zone utilizing the "root-membrane" technique: clinical results up to 5 years postloading. Int J Oral Maxillofac Implants. 2014 Nov-Dec;29(6):1397-405. doi: 10.11607/jomi.3707. Epub 2014 Sep 26. — View Citation

Tan Z, Kang J, Liu W, Wang H. The effect of the heights and thicknesses of the remaining root segments on buccal bone resorption in the socket-shield technique: An experimental study in dogs. Clin Implant Dent Relat Res. 2018 Jun;20(3):352-359. doi: 10.1111/cid.12588. Epub 2018 Feb 8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary pink esthetic score Pink esthetic score evaluates the soft tissue esthetics around implant supported crowns. Using a 0-1-2 scoring system, 0 being the lowest, 2 being the highest value. The maximum achievable PES is 14. 7 variables are measured: mesial and distal papillae being 0 if absent, 1 if incomplete and 2 if complete. Alveolar process, soft tissue level, contour, texture and color being 0 if major discrepancy, 1 if minor discrepancy and 2 if matches the contralateral 9 months
Secondary Recession of the buccal peri-implant mucosa measured at the apical zenith of the mucosal margin on the implants after digital superimposition of the optically scanned models as the vertical distance change between the former and the new position of soft tissue margins. 9 months
Secondary Corono-apical peri-implant bone dimensional changes measured at the middle of the buccal implant surface after the superimposition of Cone Beam C.T scans as the difference between the former and new vertical distance from the implant platform to the buccal alveolar crest 6 months
Secondary Bucco-lingual peri-implant bone dimensional changes measured at middle of the buccal implant surface 1mm below the alveolar crest after the superimposition of the Cone Beam C.T scans as the difference between the former and new horizontal distance between the buccal and the palatal plate of bone 6 months
Secondary Patient satisfaction: VAS Patient satisfaction will be evaluated using a questionnaire which is based on a visual analog scale (VAS). A horizontal VAS bar, 100 mm long, with the right anchor labeled "much less than natural teeth" which is marked by zero and the left anchor labeled "much more" which is marked by 10 will be used. Five questions will be formulated to record the patients' satisfaction in terms of functionality and from an esthetic point of view. Participants will look in a mirror and also be viewed a photograph before recording their answers on the horizontal calibrated line. 9 months