ClinicalTrials.gg
Status unknownNCT06170775Updated Dec 14, 2023

Sodiumhexametaphosphate as Pulp Capping Material for Primary Teeth

An interventional study of Pulp therapy and Sodiumhexametaphosphate in Pulp Disease, Dental, sponsored by Minia University. Status unknown. Open to participants aged 4 Years to 10 Years. Per ClinicalTrials.gov, last updated 2023-12-14.

Sponsored by Minia University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
4 Years to 10 Years
Sex
All
01

Study summary

Sodiumhexametaphosphate will be tested as pulp capping material in comparison to MTA for primary teeth pulp therapy

02

Conditions studied

  • Pulp Disease, Dental

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03

In context

Dental Pulp Diseases

129 studies on the registry are indexed under Dental Pulp Diseases; 39 are open to participants now.

This study's planned enrollment of 100 is above the median of 50 across 107 interventional studies indexed under Dental Pulp Diseases.

Browse Dental Pulp Diseases studies →

Lead sponsor

Minia University is the lead sponsor of 369 studies on the registry; 117 are open to participants now.

Of its 6 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
4 Years to 10 Years
Sexes eligible
All
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

  • physical healthy children
  • cooperative children
  • primary molar with deep carious lesion
  • absence of pain or transient momentary pain

Exclusion criteria

Exclusion Criteria:

  • Uncooperative children
  • children with systemic disorders
  • periapical lesions
  • sever pain
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Sodiumhexametaphosphate

    Other: Pulp therapy · Drug: Sodiumhexametaphosphate

  • Active comparator
    MTA

    Other: Pulp therapy · Other: MTA

Interventions

  • OtherPulp therapy

    Pulp capping material

  • DrugSodiumhexametaphosphate

    Sodiumhexametaphosphate

  • OtherMTA

    MTA

06

What researchers measure

Primary outcomes

  1. Clinical success

    Absence of pain, swelling and sinus tract

    Time frame: One year

  2. Radiographic success

    Absence of periapical lesions, internal or external root resorption

    Time frame: One year

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 14, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06170775
Lead sponsor
Minia University
Responsible party
Mahmoud Ahmed Mahmoud (Lecturer, Minia University) — Principal investigator
First posted
Dec 14, 2023
Start date
Dec 20, 2023 (estimated)
Primary completion
Dec 20, 2024 (estimated)
Completion
Jan 20, 2025 (estimated)
Last update
Dec 14, 2023

Oversight

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 Dec 2023. You cannot join it, but the record below documents what was studied.

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