acetaminophen
acetaminophen: 43 clinical trials tracked.
acetaminophen evidence translation
What we can confirm
43 tracked trials
What it means
What to watch
Prepared research question
What is verified about acetaminophen, and what remains unknown?
Traceable citations · Unknowns marked
See linked entities and source evidence8 indications · 11 study sponsors
Related indications
Clinical Trials (43)showing 10 most recent
Phase 2, Open-Label Study to Evaluate the Safety and Efficacy of MK-2010 in Combination With Sacituzumab Tirumotecan (Sac-TMT) in Participants With Advanced Solid Tumors
Primary endpoint: Number of Participants Who Experience an Adverse Event (AE)
A Phase 2, Open-label, Multicenter Study to Determine the Safety, Tolerability, and Efficacy of MK-1045 in Participants With Hematologic Malignancies
Primary endpoint: Cohort A Part 1: Number of Participants Who Experience Dose-Limiting Toxicity (DLT)
A Phase 1, Investigator- and Participant-Blinded, Placebo-Controlled, Randomized, Multiple-Dose Study to Evaluate the Gastric Emptying Delay, Pharmacokinetics, Safety, and Tolerability of Eloralintide in Participants With Obesity or Overweight
Primary endpoint: Acetaminophen Area Under the Concentration Versus Time Curve (AUC)
Comparing Pain Improvement for Intravenous Versus Oral Acetaminophen in Acute Pelvic Pain: A Randomized, Double-Blind, Double-Dummy Controlled Trial (PIVOTAL Trial)
Primary endpoint: Mean Change in Numeric Rating Scale (NRS) score
A Single-Centre, Open-Label Study of the Effect of UBT251 on Pharmacokinetics of an Oral Combination Contraceptive (Ethinylestradiol and Levonorgestrel) and Gastric Emptying in Women of Non-Childbearing Potential With Overweight or Obesity
Primary endpoint: AUC,EE,SS: The area under the EE plasma concentration time curve during a dosing interval at steady state
A Phase 2/3, Randomized, Open-Label, Comparison Study of MK-1045 Versus Blinatumomab in Participants With Relapsed or Refractory CD19+ B-Cell Acute Lymphoblastic Leukemia (B-ALL)
Primary endpoint: Percentage of Participants with Complete Remission (CR) in Study Part 1 and Part 2
An Investigation of the Effect of NNC0662-0419 on Pharmacokinetics of an Oral Combination Contraceptive (Ethinylestradiol and Levonorgestrel) and Gastric Emptying in Women of Non-childbearing Potential With Overweight or Obesity
Primary endpoint: Area under curve (AUC) 0-24 h, EE, steady state (SS): The area under the EE plasma concentration-time curve (pre-dose to 24 hours post-dose)
Effect of Ultrasound Guided Pecs Block With Intravenous Ketamine and Ketamine Infusion Alone For Prevention of Chronic Post-Surgical Pain in Patients Undergoing Breast Cancer Surgery: A Randomized Controlled Trial
Primary endpoint: Frequency of Chronic Post-operative Pain
Antipyretic Therapy With and Without Cold Sponging: A Comparative Study in Febrile Children.
Primary endpoint: Fever reduction
Optimizing Pain Treatment in Children On Mechanical Ventilation
Primary endpoint: Acute Pain Episodes