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New treatment option for Post Operative Pain Management
Official title Influence of Occlusal Reduction on Endodontic Postoperative Pain
ClinicalTrials.gov ID: NCT06977009
What this study is testing
- What it's testing
- This study aims to assess the impact of occlusal reduction on post-operative pain after single-visit root canal treatment in patients with necrotic pulps or previously initiated (accessed).
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 70
You may be able to join if
- Systemically healthy people (ASA I\&II) between the age of 18 and 70 years
- Patients diagnosed with necrotic pulp or previously initiated (accessed).
- Posterior maxillary or mandibular molar tooth.
- Presence of an opposing tooth (or teeth) with normal occlusal contact with the opposing tooth (or teeth).
- Tooth needs cuspal coverage.
You likely can't join if
- Pregnant females.
- Patients with significant medical conditions (ASA III \& IV).
- Reported bruxism or clenching.
- Took analgesics\\antibiotics or other drugs that might alter their pain during the last 12 hours preoperatively.
- A history of allergic reactions to any of the medications and/or materials used.
- Patients with a tooth that had no contacts or premature contact, fewer than three teeth on one side of the jaw.
See the full eligibility criteria
- Systemically healthy people (ASA I\&II) between the age of 18 and 70 years
- Patients diagnosed with necrotic pulp or previously initiated (accessed).
- Posterior maxillary or mandibular molar tooth.
- Presence of an opposing tooth (or teeth) with normal occlusal contact with the opposing tooth (or teeth).
- Tooth needs cuspal coverage.
- Pregnant females.
- Patients with significant medical conditions (ASA III \& IV).
- Reported bruxism or clenching.
- Took analgesics\\antibiotics or other drugs that might alter their pain during the last 12 hours preoperatively.
- A history of allergic reactions to any of the medications and/or materials used.
- Patients with a tooth that had no contacts or premature contact, fewer than three teeth on one side of the jaw.
- Greater than grade I mobility or pocket depth greater than 5mm.
- Non-restorable crowns, severely curved root canals, or post-treatment endodontic disease were, also, excluded.
The study team makes the final eligibility decision.
Where it's taking place
- Amman, Amman Governorate, Jordan
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 70 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Amman, Amman Governorate, Jordan. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.