Effect of Occlusal Reduction on Post-operative Pain

Apical Periodontitis Clinical Trial

Official title:

Effect of Occlusal Reduction on Post-operative Pain in Patients With Irreversible Pulpitis and Symptomatic Apical Periodontitis Treated in a Single-visit: A Randomized Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03189771
• Other study ID #: evidence comittee
• Status: Not yet recruiting
• Phase: N/A
• First received: June 9, 2017
• Last updated: June 15, 2017
• Start date: June 27, 2017
• Est. completion date: July 30, 2018

Study information

• Verified date: June 2017
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

effect of occlusal reduction on post-operative pain is evaluated after single visit root canal treatment in upper and lower molar teeth in patients with sypmtomatic irreversible pulpitis and apical periondontis

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 52
• Est. completion date: July 30, 2018
• Est. primary completion date: July 1, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 50 Years

Eligibility

Inclusion Criteria:

1. Patient's age between 20-50 years with no sex predilection.

2. Medically free patients.

3. Patients suffering from symptomatic irreversible pulpitis with symptomatic apical periodontitis in maxillary and mandibular molars with:

• Preoperative pain.

• Vital pulp.

• Sensitivity to percussion.

• Occlusal contact with the opposing teeth.

• Normal periapical radiographic appearance or slight widening in the periodontal membrane space.

Exclusion Criteria:

1. Pregnant females.

2. Patients having a significant systemic disorder.

3. Patients who had administered analgesics or antibiotics during the last 12 hours preoperatively.

4. Patients having bruxism or clenching.

5. Teeth having :

• No occlusal contact.

• No sensitivity to percussion.

• Association with swelling or fistulous tract.

• Acute or chronic peri-apical abscess.

• Greater than grade I mobility.

• Pocket depth greater than 5mm.

• No possible restorability.

• Previous endodontic treatment

Related Conditions & MeSH terms

• Apical Periodontitis
• Evaluate Occlusal Reduction on Post-operative Pain
• Pain, Postoperative
• Periapical Periodontitis
• Periodontitis
• Pulpitis
• Teeth With Symptomatic Irreversible Pulpitis

Intervention

Procedure:
• occlusal surface reduction
occlusal surface reduction after single visit root canal treatment

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	pre-operative pain before single visit root canal treatment by NRS (numerical rating scale)	Primary outcome will be assessed by NRS (numerical rating scale), the unit of measurement is categorical.The scale is from (0-10) (1-3) Mild pain (4-6) Moderate pain (7-10) Severe pain	Baseline
Primary	post-operative pain after single visit root canal treatment by NRS (numerical rating scale)	Primary outcome will be assessed by NRS (numerical rating scale), the unit of measurement is categorical.The scale is from (0-10) (1-3) Mild pain (4-6) Moderate pain (7-10) Severe pain	after treatment by 6 hours
Primary	post-operative pain after single visit root canal treatment by NRS (numerical rating scale)	Primary outcome will be assessed by NRS (numerical rating scale), the unit of measurement is categorical.The scale is from (0-10) (1-3) Mild pain (4-6) Moderate pain (7-10) Severe pain	after treatment by 12 hours
Primary	post-operative pain after single visit root canal treatment by NRS (numerical rating scale)	Primary outcome will be assessed by NRS (numerical rating scale), the unit of measurement is categorical.The scale is from (0-10) (1-3) Mild pain (4-6) Moderate pain (7-10) Severe pain	after treatment by 24 hours
Primary	post-operative pain after single visit root canal treatment by NRS (numerical rating scale)	Primary outcome will be assessed by NRS (numerical rating scale), the unit of measurement is categorical.The scale is from (0-10) (1-3) Mild pain (4-6) Moderate pain (7-10) Severe pain	after treatment by 48 hours