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Active, not recruitingNCT06785961(EIRR)Updated Jan 21, 2025

Healing Assessment of External Inflammatory Root Resorption After Revascularization Technique of Avulsed Permanent Central Incisor (Case Study)

A Phase 1 interventional study of Regeneration of traumatic tooth in Avulsion, sponsored by Badr University. Active, not recruiting at 1 site in Egypt. Open to male participants aged 11 Months and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-01-21.

Sponsored by Badr University · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Aug 2025, 1 year 2 months ago, but the record still lists the study as active, not recruiting.
Phase
Phase 1
Study type
Interventional
Enrollment
4
Allocation
Not applicable
Ages
11 Months and older
Sex
Male
01

Study summary

Evaluate the healing of external root resorption of replanted avulsed permanent maxillary central incisor after revascularization.

Read the detailed description

Healing assessment of external inflammatory Root Resorption after Revascularization Technique of Avulsed permanent Central Incisor (Case study)

02

Conditions studied

  • Avulsion

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03

In context

Fractures, Avulsion

16 studies on the registry are indexed under Fractures, Avulsion; 4 are open to participants now.

Browse Fractures, Avulsion studies →

Lead sponsor

Badr University is the lead sponsor of 64 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
11 Months and older
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • traumatic teeth
  • external inflammatory root resorption

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
4 participants (actual)

Study arms

  • Experimental
    Single- arm

    Case study

    Procedure: Regeneration of traumatic tooth

Interventions

  • ProcedureRegeneration of traumatic tooth

    Revascularization is a new treatment method for immature necrotic , pulp revascularization allows also the stimulation of the apical development and the root maturation of immature teeth ( growth and thickening of dentinal walls ).

06

What researchers measure

Primary outcomes

  1. Measure amount of bone healing and root formation by using cone beam computed tomography (CBCT)

    Measure amount of bone healing and root formation by using measuring tool cone beam computed tomography (CBCT) By using measuring unit hounsfield unit (HU)

    Time frame: 18 months

Secondary outcomes

  1. Measuring pain by using the numeric pain rating scale

    Measuring pain by using the numeric pain rating scale, through patient is asked to make three pain rating, the average of three ratings was used to represent the patient's level of pain (0 none) (1-3 mild) (4-6 moderate) (7-10 severe)

    Time frame: 18 months

  2. Pulp test to assess the vitality or health of the dental pulp

    Pulp test to assess the vitality or health of the dental pulp through measuring tool thermal pulp test :applied to the tooth to assess the response. The unit of measurement here is typically °C (degrees Celsius) .

    Time frame: Every 6 months

07

Study locations

1 site
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Nov 2024 (actual). Primary completion is estimated for Aug 2025, 9 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 8, 2024
First posted
Jan 21, 2025
StartActual
Nov 27, 2024
Primary completionEst.
Aug 31, 2025
CompletionEst.
Aug 31, 2025
Last update
Jan 21, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 21, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06785961
Lead sponsor
Badr University
Responsible party
Abdelrhaman Reda Elshair (Teaching assistant at badr university in cairo, Badr University) — Principal investigator
First posted
Jan 21, 2025
Start date
Nov 27, 2024
Primary completion
Aug 31, 2025 (estimated)
Completion
Aug 31, 2025 (estimated)
Last update
Jan 21, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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