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Single vs. Double Tenting Screws for Horizontal Ridge Augmentation.

O

Omar Saad

Status

Completed

Conditions

Bone Defects

Treatments

Procedure: horizontal bone augmentation using Double tenting screw
Procedure: horizontal bone augmentation using single tenting screw

Study type

Interventional

Funder types

Other

Identifiers

NCT07060027
4/626/88/2022

Details and patient eligibility

About

The goal of this clinical trial is to learn if using two screws works better than one screw for building up jawbone width before dental implant placement. It will also check the safety of both techniques. The main questions it aims to answer are:

  • Does using two screws give better bone growth than using one screw?
  • Which technique creates more stable bone for dental implants?

Researchers will compare the single-screw technique to the double-screw technique to see which works better for jawbone reconstruction.

Participants will:

  • Receive either one or two small titanium screws placed in their jawbone to support a bone graft
  • Have the graft covered with a protective membrane
  • Return after 6 months for screw removal and dental implant placement
  • Attend follow-up visits to check healing progress

The study will help dentists determine the best method for patients who need jawbone reconstruction before getting dental implants. All procedures use FDA-approved materials and follow standard surgical protocols.

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Enrollment

16 patients

Sex

All

Ages

20 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients are systemically healthy based on questionnaire dental modification of Cornell index (Bolender, C. L. et al., 1969).
  • Gingival health according to the new classification system (Caton, J. G. et al., 2018).
  • The recipient site of the augmentation is free from any pathological conditions.
  • At least 1 tooth area with a ridge defect and planned to receive a dental implant. The site must be bordered by at least 1 tooth.
  • Class I ridge defect according to Seibert's classification.
  • Adequate interocclusal space to accommodate the available restorative components.

Exclusion criteria

  • Parafunctional habits such as bruxism and clenching
  • Smokers
  • Pregnant females

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

16 participants in 2 patient groups

Single tenting screw
Experimental group
Description:
8 patients indicated for lateral ridge augmentation in premolar-molar area (class I Seibert's classification) will be candidates to screw tent technique using single screw at crest position
Treatment:
Procedure: horizontal bone augmentation using single tenting screw
Double tenting screw
Active Comparator group
Description:
8 patients indicated for lateral ridge augmentation in premolar-molar area (class I Seibert's classification) will be candidates to screw tent technique using double screws, one at a crestal position and the other one 5 mm apical to the first one.
Treatment:
Procedure: horizontal bone augmentation using Double tenting screw

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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