Skip to content

The Effect of Different Intra-canal Medications on Postoperative Pain

Evaluation of Postoperative Pain After Using Ibuprofen, Nitrofurantoin, or Calcium Hydroxide as Intracanal Medicaments in Root Canal Treatment of Necrotic Mandibular Posterior Teeth. A Randomized Controlled Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07603934
Enrollment
111
Registered
2026-05-22
Start date
2025-12-15
Completion date
2027-03-15
Last updated
2026-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulp Necrosis, Apical Periodontitis

Keywords

Necrotic Pulp

Brief summary

The aim of this study is to assess the effect of ibuprofen, nitrofurantoin, and calcium hydroxide on postoperative pain after endodontic treatment of necrotic mandibular posterior teeth Research question/hypothesis: In patients with necrotic pulps in their mandibular posterior teeth, there would be no difference in the incidence and/or severity of postoperative pain after the use of ibuprofen, nitrofurantoin, or calcium hydroxide intracanal medications. The study will evaluate postoperative pain after using either of the tested drugs as an intracanal medication amidst visits. of endodontic treatment in cases where pulp necrosis is confirmed.

Detailed description

* Trial design: * A Randomized controlled, double-blind, parallel-arm, clinical trial. * Allocation ratio 1:1:1 * Framework: superiority * Study settings: Outpatient clinic of Endodontics at the Faculty of Dentistry, Egyptian Russian University, Badr city, Cairo governorate, Egypt. * Eligibility criteria * Inclusion criteria: 1. Patients with necrotic pulps. 2. Adult, healthy patients, older than 18 years old 3. Males and females. 4. Patient with the ability to understand and use pain scales. 5. Patient who accepts enroll to the study. * Exclusion criteria: 1. Patients' allergies or any other contraindication to any of the medications used. 2. Pregnant and lactating females. 3. Patients have been taking pain medication 12 hours earlier. 4. Patients who have more than one symptomatic mandibular tooth in the same quadrant. 5. Patients with contributory medical history (ASA\>II). * Diagnosis: The diagnosis of pulp necrosis is confirmed through the patients' history, lack of response to cold testing and negative response to electric pulp tester whenever .The treatment will be done on two- visits. • Treatment procedure: Each patient will be given an NRS chart to rate her /his presenting pain as preoperative pain. After complete mechanical preparation, each patient will be randomly assigned to either of three groups as follows, group 1: ibuprofen will be used as an intracanal medication, group 2: nitrofurantoin will be used as an intra canal medication and group 3: CaOH will be used as an intracanal medicament. The access cavity will be then sealed with temporary filling (MD-TEMP, META BIOMED CO., LTD. Chungbuuk, Korea). Post-operative instructions and appropriate post-operative rescue medication will be prescribed (400mg Ibuprofen). All patients will be asked to record their postoperative pain level felt on NRS at 6, 12, 24, 48, 72 hours and 7 days. One week after the first visit, patients will be recalled to the clinic to complete their root canal treatment as recommended. All canals will be dried then obturated by the modified single cone technique using 0.04 taper gutta percha points and epoxy resin sealer. Patients will be referred to an operative or a fixed prosthodontics specialist for crown placement at the Faculty of Dentistry, Egyptian Russian University. Research objective (state the aim) The aim of this study is to assess the effect of ibuprofen, nitrofurantoin and calcium hydroxide on postoperative pain after endodontic treatment of necrotic mandibular posterior teeth. Sample size: (if calculation equation is used please state) A total of 111 patients, 37 per group needed for the clinical trial was calculated Grouping & Randomization used:(specify if present) Three groups Group 1: ibuprofen Group 2: nitrofurantoin Group 3: calcium hydroxide Outcome variables: The primary outcome the effect of ibuprofen, nitrofurantoin and calcium hydroxide on postoperative pain after endodontic treatment of necrotic mandibular posterior teeth. Postoperative pain will be measured using NRS at 6, 12, 24, 48, 72 hours postoperatively. Numerical Rating Scale (NRS) (20): It is an 11-point scale consisting of numbers from 0 through 10; - 0 reading represents "no pain" - 1-3 readings represent "mild pain" - 4- 6 readings represent "moderate pain" - 7- 10 readings represent "severe pain"

Interventions

DRUGibuprofen

Ibuprofen. a NSAID, will be ground and formed into a paste to be placed inside the root canals of necrotic mandibular posterior teeth, to explore its effects on post-operative pain

DRUGNitrofurantoin

Nitrofurantoin tablets will be formed into a paste to be placed inside the root canals of necrotic mandibular premolars during endodontic treatment.

DRUGCalcium Hydroxide

Calcium Hydroxide intracanal medicament will be placed inside the root canals of mandibular necrotic posterior teeth during endodontic treatment.

Sponsors

Cairo University
Lead SponsorOTHER
Egyptian Russian University
CollaboratorNETWORK
Fayoum University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Masking Description

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patients with necrotic pulps. 2. Adult, healthy patients, older than 18 years old 3. Males and females. 4. Patient with the ability to understand and use pain scales. 5. Patient who accepts enroll to the study.

Exclusion criteria

1. Patients' allergies or any other contraindication to any of the medications used. 2. Pregnant and lactating females. 3. Patients have been taking pain medication 12 hours earlier. 4. Patients who have more than one symptomatic mandibular tooth in the same quadrant. 5. Patients with contributory medical history (ASA\>II).

Design outcomes

Primary

MeasureTime frameDescription
Intensity of Postoperative painBaseline (preoperative) and at 6, 12, 24, 48 and 72 hours after placement of the intracanal medicament.Postoperative pain intensity will be self-reported by patients using an 11-point Numerical rating scale (NRS), where 0 represents "no paon" and 10 represents "the worst immaginable pain"

Secondary

MeasureTime frameDescription
Incidence of Postoperative painUp to 72 hours after placement of intracanal medicamentThe percentage of patients experiencing any postoperative pain (NRS=0) within the follow-up period
Postoperative Analgesic ConsumptionUp to 72 hours postoperativelyThe total amount of prescribed analgesics consumed by the oatient. this will be measured by counting the total number of Ibuprofen 400 mg tablets taken by patients.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 22, 2026