Trials / Unknown
UnknownNCT04338633
Post-operative Pain Reduction
Post-operative Pain Reduction After Application of Three Intracanal Medicament Within Necrotic Root Canals and Pulp
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- Sponsor
- Minia University · Academic / Other
- Sex
- All
- Age
- 25 Years – 50 Years
- Healthy volunteers
- Accepted
Summary
Recruited patients with necrotic pulp after application of conventional calcium hydroxide paste are assigned to group, Calcium hydroxide nanoparticle group and Combined Calcium hydroxide with silver nanoparticle group and record postoperative pain afterwards.
Detailed description
The investigator will recruit patients who are found eligible to the criteria, conventional calcium hydroxide paste , Calcium hydroxide nanoparticle and Combined Calcium hydroxide with silver nanoparticle . After 48 hours, patients will be randomly assigned to removal of intracanal medication After the visit, patients will be asked to record post operative pain by Numerical Rating Scale)in a given sheet
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Conventional calcium hydroxide paste | Conventional calcium hydroxide paste (Ultracal) will be removed in second visit. |
| DRUG | Calcium hydroxide nanoparticle | Calcium hydroxide nanoparticle. manufactured in NanoTech. institute, will be removed in second visit. |
| DRUG | Combined Calcium hydroxide with silver nanoparticle | Combined Calcium hydroxide with silver nanoparticle will be removed in second visit. |
Timeline
- Start date
- 2020-04-01
- Primary completion
- 2020-11-01
- Completion
- 2020-11-01
- First posted
- 2020-04-08
- Last updated
- 2020-04-08
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04338633. Inclusion in this directory is not an endorsement.