Phase 4 Volume Clinical Trials
8 recruitingPhase 4
What is a Phase 4 trial?
Phase 4 trials, also called post-marketing studies, are conducted after a treatment has been approved and is available to the public. They monitor long-term effectiveness and safety in a broader population.
Showing 1–8 of 8 trials
Recruiting
Phase 4
Restoring Facial Volume After GLP-1 Weight Loss With Radiesse
Volume Loss (Soft Tissue Ptosis or Atrophy )
Kalpna Kay Durairaj, MD, FACS48 enrolled1 locationNCT07419854
Recruiting
Phase 4
Application of Topical Oxygen Therapy Around Customized Healing Collar
Soft TissueHealing Abutment Influence on Gingival VolumeSoft Tissue Healing+1 more
Cairo University6 enrolled1 locationNCT07384403
Recruiting
Phase 4
Gator SCALES-WHF: SubCutaneous Administration of Lasix to Eliminate Symptoms of Worsening Heart Failure
Heart FailureVolume Overload
University of Florida100 enrolled1 locationNCT06979726
Recruiting
Phase 4
Determination of the Optimal Volume of Liposomal Bupivacaine in Adductor Canal Block for Knee Joint Surgery
Optimal Volume of Liposomal Bupivacaine
Nanjing First Hospital, Nanjing Medical University63 enrolled1 locationNCT06942689
Recruiting
Phase 4
HighCycle Study: Acetazolamide, High Altitude and Plasma Volume
WomenHigh Altitude EffectsHigh Altitude Hypoxia+2 more
Centre d'Expertise sur l'Altitude EXALT270 enrolled1 locationNCT07118462
Recruiting
Phase 4
Efficacy and Safety of Combination Diuretic Therapy in Patients With Acute Decompensated Heart Failure and Volume Overload
EdemaAcute Decompensated Heart FailureVolume Overload
Cairo University110 enrolled1 locationNCT06414759
Completed
Phase 4
Evaluation of intravenous fluid resuscitation with either 4% albumin or 20% albumin solution for patients admitted to the intensive care unit
Low blood volume states
Austin Health400 enrolled2 locationsACTRN12615000349549
Completed
Phase 4
Evaluation of performance of cuffed and uncuffed endotracheal tubes in a paediatric population: A randomised controlled trial.
We hypothesise that the rate of respiratory complications will be similar between the groups receiving either cuffed or uncuffed endotracheal tubes.We hypothesize that there will be a higher rate of endotracheal tube leak in uncuffed compared with cuffed tubes, and that the rate of sore throat will be higher in the uncuffed group.We furthermore hypothesise that the loss in lung volume following a standardized recruitment maneouver will be greater in the children intubated with uncuffed ETTs as compared with cuffed ETTs.
Princess Margaret Hospital for Children104 enrolled1 locationACTRN12612000045819