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Status unknownNCT05341245Updated Apr 22, 2022

Graphene Oxide in the Surgical Management of Intrabony Periodontal Defects

An interventional study of Graphene oxide and open flap debridement and Open flap debridement in Periodontal Diseases, sponsored by Ain Shams University. Status unknown. Open to male participants aged 1 Year to 2 Years. Per ClinicalTrials.gov, last updated 2022-04-22.

Sponsored by Ain Shams University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Apr 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
6
Allocation
Randomized
Ages
1 Year to 2 Years
Sex
Male
01

Study summary

Using Graphene oxide in the surgical management of periodontal intrabony defects.

Read the detailed description

Evaluation of the effect of Graphene oxide in the surgical management of periodontal intrabony defects in animals in periodontal clinical parameters with histomorphometric evaluation .

02

Conditions studied

  • Periodontal Diseases

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03

In context

Periodontal Diseases

855 studies on the registry are indexed under Periodontal Diseases; 189 are open to participants now.

This study's planned enrollment of 6 is below the median of 45 across 546 interventional studies indexed under Periodontal Diseases.

Browse Periodontal Diseases studies →

Lead sponsor

Ain Shams University is the lead sponsor of 1,930 studies on the registry; 433 are open to participants now.

Of its 33 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
1 Year to 2 Years
Sexes eligible
Male
Accepts healthy volunteers
No

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

  • male dogs
  • 12-24 months old with approximate weight of 20-30 kg and general good health will be used

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
6 participants (estimated)

Study arms

  • Experimental
    Graphene oxide group

    The surgical defect will be managed by open flap debridement and application of Graphene oxide

    Procedure: Graphene oxide and open flap debridement

  • Other
    Open flap group

    The surgical defect will be managed by open flap debridement

    Procedure: Open flap debridement

Interventions

  • ProcedureGraphene oxide and open flap debridement

    Using Graphene oxide with open flap debridement in management of periodontal intrabony defects in dogs

  • ProcedureOpen flap debridement

    Using Open flap debridement in management of periodontal intrabony defects in dogs

06

What researchers measure

Primary outcomes

  1. periodontal probing depth

    To evaluate the use of Graphene Oxide in the surgical management of intrabony periodontal defects regarding the changes in periodontal probing depth "measured in mm " using University of North Carolina periodontal probe( UNC 15 probe ).

    Time frame: 2 months

  2. Clinical attachment level

    To evaluate the use of Graphene Oxide in the surgical management of intrabony periodontal defects regarding the changes in clinical attachment level "measured in mm " using University of North Carolina periodontal probe( UNC 15 probe )

    Time frame: 2 month

Secondary outcomes

  1. Histomorphometric evaluation

    To evaluate the use of Graphene Oxide in the surgical management of intrabony periodontal defects using histological sections obtained from the surgical site to do quantitative assessment of bone remodeling, modeling, and structure by "counting the number of osteoblasts and the number of bone trabeculae " using computer based microscope and software.

    Time frame: 2 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for May 2022; primary completion for May 2023, 12 months later.

Of 308 non-industry interventional studies with no phase under Periodontal Diseases, half reached primary completion within 13 months of starting (the median), counting those still running; a quarter within 7 and three quarters within 26. This study's planned 12 months is close to that.

Counting every sponsor, half of 326 studies reached it within 13 months; a quarter within 7 and three quarters within 25.

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

Registered
Mar 22, 2022
First posted
Apr 22, 2022
StartEst.
May 1, 2022
Primary completionEst.
May 1, 2023
CompletionEst.
Jun 1, 2023
Last update
Apr 22, 2022
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 Apr 22, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05341245
Responsible party
Zeiad Khaled (Principal investigator, Ain Shams University) — Principal investigator
First posted
Apr 22, 2022
Start date
May 1, 2022 (estimated)
Primary completion
May 1, 2023 (estimated)
Completion
Jun 1, 2023 (estimated)
Last update
Apr 22, 2022

Study contacts

Zeiad Rashad
Contact
Zeiadkhaled2010@gmail.com
2001111309030

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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