Post Operative Pain Clinical Trial
Official title:
Effect of Ascorbic Acid as a Final Flush on Post-operative Pain After Single Visit Root Canal Treatment for Patients With Symptomatic Irreversible Pulpits Related to Mandibular Molars: Randomized Controlled Trial.
The study is conducted to evaluate the effect of Ascorbic acid as a final flush on post operative pain after single visit root canal treatment in cases with symptomatic irreversible pulpits.
Status | Not yet recruiting |
Enrollment | 30 |
Est. completion date | August 2023 |
Est. primary completion date | August 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Patients above 18 years old and to 60. - Male or female. - Patients seeking root canal treatment. - mandibular molar teeth with symptomatic irreversible pulpits with preoperative acute or moderate pain with hot and cold stimulation with normal periapical radiographic appearance . - healthy patient (ASA I,II). - Patient who can understand NRS and sign informed consent. Exclusion Criteria: - Medically compromised patients having significant systemic disorders. (ASA III or IV). - History of intolerance to NSAIDS. - External root resorption. - Internal root resorption. - Vertical root fracture. - Periapical lesion. - Pregnancy. - Use of ibuprofen in the last 12 hour. - Bleeding disorder. - Long term corticosteroid use. - Mobility Grade II or III. - Pocket depth more than 5mm. - Previous root canal therapy. - Non-restorability. - TMJ problems, bruxism, clenching or traumatic occlusion. - Inability to perceive the given instructions. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain intensity measured by numerical rating scale where 0= no pain, 1-3= mild pain, 4-6= moderate pain and 7-10= severe pain. | up to 48 hours after root canal treatment. | ||
Secondary | If there are analgesics taken by the patient after root canal treatment and that will be measured by a questionnaire. | up to 48 hours. |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05619796 -
Assessment of Clinical & Radiographic Efficiency of Manual & Pediatric Rotary Systems in Primary Root Canal Preparation
|
N/A | |
Recruiting |
NCT05338671 -
Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment
|
Phase 4 | |
Completed |
NCT05584696 -
Effectiveness of Green Color Exposure on Dental Anxiety
|
N/A | |
Completed |
NCT05593341 -
Opioid Education in Total Knee Arthroplasty
|
N/A | |
Not yet recruiting |
NCT05255146 -
Cryoanalgesia and Post-thoracotomy Pain in Minimally Invasive Cardiothoracic Surgery
|
N/A | |
Not yet recruiting |
NCT06020196 -
The Safety and Efficacy of Surgical Rectus Sheath Block for Postoperative Analgesia After Elective Cesarean Delivery
|
N/A | |
Completed |
NCT01697748 -
Prospective Study on Cesarean Wound Outcomes
|
N/A | |
Completed |
NCT01681966 -
A Single-dose Open-Label Study to Assess the Safety and Preliminary Efficacy of PRF 110 in Open Herniorrhaphy Surgery
|
Phase 2 | |
Completed |
NCT01442818 -
Patient Satisfaction and Pain Control Following Reconstructive Vaginal Surgery
|
N/A | |
Completed |
NCT00625911 -
Ketamine Improves Post-Thoracotomy Analgesia
|
N/A | |
Terminated |
NCT05494125 -
Effects of Continuous ESP Catheters on Recovery, Pain and Opioid Consumption After Multilevel Spine Surgery
|
N/A | |
Recruiting |
NCT04767399 -
Comparison of Postoperative Pain After Instrumentation in Different Visits With Different Single File Systems.
|
N/A | |
Not yet recruiting |
NCT05863624 -
Open and Endoscopic Technique in Female Inguinal Hernia Repair. FemaleHernia
|
N/A | |
Completed |
NCT06048744 -
Ultrasound Guided Erector Spinae Plane Block vs External Oblique Intercostal Plane Block for Nephrectomy
|
N/A | |
Active, not recruiting |
NCT05374499 -
Double-Blinded Randomized Controlled Study Investigating the Efficacy of Exparel (Liposomal Bupivacaine) for Postoperative Pain Relief in Mandibular Third Molar Extractions
|
Phase 4 | |
Completed |
NCT06082479 -
The Effect of Intra Oral Cryotherapy in Patients With Symptomatic Apical Periodontitis
|
N/A | |
Completed |
NCT05552391 -
Dexametomedine Versus Ketamine as an Adjuvant in Erector Spinae Block for Perioperative Thoracotomy Pain Control
|
Phase 4 | |
Completed |
NCT06065683 -
Acute Postoperative Pain Prevalence and Intensity in the First 72 Hours
|
||
Completed |
NCT05510947 -
Acute Postoperative Pain and Catastrophizing in Patients Undergoing Unicompartmental Knee Arthroplasty
|
||
Recruiting |
NCT04909060 -
Does the Newborn Infant Parasympathetic Evaluation (NIPE) Index Predict Postsurgical Pain in Children
|