NCT03626779

Brief Summary

Atrumatic extraction ,immediate implant placment , prf as plug,immediate loading , mesure bone density 0-3-6-9 month

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2018

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 30, 2018

Completed
14 days until next milestone

First Posted

Study publicly available on registry

August 13, 2018

Completed
19 days until next milestone

Study Start

First participant enrolled

September 1, 2018

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2019

Completed
Last Updated

August 22, 2018

Status Verified

August 1, 2018

Enrollment Period

12 months

First QC Date

July 30, 2018

Last Update Submit

August 21, 2018

Conditions

Bone Density Increased

Outcome Measures

Primary Outcomes (1)

  • Bone density enhancement with prf in immediate implant placment and loding

    Cbct

    9 month

Study Arms (2)

immediate placment and loading with prf

OTHER

Immediat placment and loading with prf

Other: Prf

immediate implant placment and loading

NO INTERVENTION

Immediate implant placment and loading without prf

Interventions

PrfOTHER

Take 10cc blood from patient and gain prf blug

immediate placment and loading with prf

Eligibility Criteria

Age20 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • unrestorable anterior tooth.
  • Good oral hygine
  • Adequate bone hieght apical to the alveolus of failing tooth to ensure primary stability .

You may not qualify if:

  • systematic disease which affect osteointgration.
  • Bad oral hygiene
  • Broxism, clenching, deep bite, edge to edge and abnormal habits.
  • Non-treated peeiodontal diseases.
  • Pregnancy and smokers. Severe infection. Loss of labial crest after extraction of failing tooth.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Osteosclerosis

Interventions

Prolactin-Releasing Hormone

Condition Hierarchy (Ancestors)

OsteochondrodysplasiasBone Diseases, DevelopmentalBone DiseasesMusculoskeletal Diseases

Intervention Hierarchy (Ancestors)

Hypothalamic HormonesPeptide HormonesHormonesHormones, Hormone Substitutes, and Hormone AntagonistsNeuropeptidesPeptidesAmino Acids, Peptides, and ProteinsNerve Tissue ProteinsProteins

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
CairoU

Study Record Dates

First Submitted

July 30, 2018

First Posted

August 13, 2018

Study Start

September 1, 2018

Primary Completion

August 30, 2019

Study Completion

August 30, 2019

Last Updated

August 22, 2018

Record last verified: 2018-08