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Completed

NCT Number: NCT05321589

Accuracy of Conventional and Digital Impression Techniques Used for Maxillary Hybrid Prosthesis

evaluation and comparison of the accuracy of conventional and digital impression for full arch screw retained prosthesis for edentulous maxilla.

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Key information

Age range

50 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

faculty of Dentistry , Mansoura University

Al Mansurah, DK, 35516, Egypt

About this study

Each patient received 6 implants in the maxillary ridge (widely distributed across the arch) in the following positions: central incisors, canines/first premolar teeth and first molar teeth aided by surgical stent. then each patient received 2 types of impression techniques Technique 1 :conventional impression conventional open tray impression technique with splinted transfers using vinylpolysiloxane and Technique2 : Digital impression taken using original scan bodies torqued to the implants .three dimensional accuracy of impression techniques was evaluated using linear measurements and 3D deviation between the two techniques was measured.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The patients were selected according to the following inclusion criteria:
  • Completely edentulous maxillary and mandibular ridges
  • Healthy ridge covered by normal oral mucosa and free from any ridge flabbiness.
  • All of the patients were dissatisfied with the retention and stability of their maxillary conventional dentures and expressed a strong desire for a more stable prosthesis.
  • Sufficient bone quantity and quality in the front and posterior maxillary regions, as determined by preoperative CBCT, to accommodate six implants with a diameter of at least 3.5 mm and a length of at least 10 mm.
  • Enough restorative space (from the mucosa covering the crest of the maxillary residual ridge to the occlusal plane) to allow the fixed prosthesis to be constructed ,preliminary jaw relationship revealed this.
  • It's been at least a year since the last extraction.

Exclusion criteria

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  • Systemic diseases that may alter tissue response to implantation and affects osseointegration (radiation, diabetes, osteoporosis, bleeding disorders or hepatic patients)
  • Long term immunosuppressive and corticosteroid drug therapy.
  • Patient with abnormal habits as clenching and bruxism.
  • Smoking patients.
  • Patients with problems in TMJ.
  • Neuromuscular diseases.

Treatment and study plan

impression techniques for implant used for maxillary screw retained hybrid prosthesis

Other

conventional splinted open tray impression technique was done for maxillary implants to fabricate screw retained hybrid prosthesis and digital intra oral impression was done for the same patients after screwing scan bodies to the implants intra orally.

evaluation of accuracy and 3D deviation between the two techniques was done

Other names: digital and conventional impression techniques

Primary outcomes

  1. accuracy of impression technique

    Time frame: immediately after the intervention/procedure

    deviation measurements digitally

Secondary outcomes

  1. passivity of final restoration

    Time frame: immediately after the intervention/procedure

    Clinical measurement of prosthesis passivity using single screw test of Sheffield.

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Official study title

Accuracy of Digital and Conventional Impression Techniques for Maxillary Full Arch Screw Retained Hybrid Prosthesis

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Apr 11, 2022
Registry last updated
Apr 11, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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