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Completed

NCT Number: NCT03032978

Calcium Silicate Versus Calcium Hydroxide in Two-step Indirect Pulp Treatment

Clinical and microbiological evaluation of Calcium silicate versus Calcium hydroxide in two-step indirect pulp treatment: Randomized clinical trial

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Key information

Conditions

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ehsan Hossam

Cairo, Giza Governorate, 12345, Egypt

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • 18-50 years.
  • Males or females.
  • Co-operative patients approving to participate in the trial.

Exclusion criteria

  • Patients younger than 19 years old or older than 50 years old.
  • Disabilities.
  • Systemic diseases or severe medically compromised.
  • Lack of compliance.

Treatment and study plan

Calcium hydroxide

Other

Pulp capping material

Other names: Dycal

Calcium silicate

Other

Pulp capping material

Other names: Theracal

Primary outcomes

  1. Pain: VAS

    Time frame: 6 month

    post operative pain after 6 month from material application will be measured by visual analogue scale (VAS)with score from 0 to 10 in which 0 means no pain and 10 means the worst pain

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Clinical and Microbiological Evaluation of Calcium Silicate Versus Calcium Hydroxide in Two-step Indirect Pulp Treatment: Randomized Clinical Trial

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Jan 26, 2017
Registry last updated
Jan 27, 2020

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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