Nausea and Vomiting, Postoperative
Conditions
Brief summary
Randomized, double-blind, pediatric trial of amisulpride for prophylaxis of post operative nausea and vomiting
Detailed description
Randomized, double-blind, Phase 2/3 study of IV amisulpride as prevention of post-operative nausea and vomiting in pediatric patients
Interventions
Dose finding treatment for continuation to phase 3
DRUGDexamethasone
Standard of care treatment
Sponsors
Amicus CD LLC
Premier Research
Acacia Pharma Ltd
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
2 Months to 17 Years
Healthy volunteers
No
Inclusion criteria
1. Male or female patients aged from full-term birth to 17 years of age 2. Signed informed consent form and/or assent and willingness of patient and parents to participate in the trial 3. Patients undergoing non-emergency surgery, preferentially eye surgery, adenotonsillectomy or otoplasty, under general anesthesia (other than total intravenous anesthesia with propofol) expected to last at least 30 minutes from induction of anesthesia to removal of Endotracheal tube (ETT) or Laryngeal mask airway (LMA) 4. American Society of Anesthesiologists (ASA) risk score I-III 5. For females of child-bearing potential: ability and willingness to use a highly effective form of contraception (as defined in ICH M3 guidance, e.g., true (not periodic) abstinence from sexual intercourse, surgical sterilization (of subject or partner), combined oral contraceptive pill, or any other method or combination of methods with a failure rate generally considered to be \<1% per year) between the date of screening and at least 48 hours after administration of study drug.
Exclusion criteria
1. Patients scheduled to undergo transplant or Central Nervous System (CNS) surgery 2. Patients scheduled to receive only a local anesthetic and/or regional neuraxial (intrathecal or epidural) block (without general anesthesia) or to receive general anesthesia involving total intravenous anesthesia (TIVA) with propofol 3. Patients who, in the opinion of the Investigator, are expected to remain ventilated for a significant period after surgery 4. Patients who are expected to need a naso- or orogastric tube in situ after surgery is completed 5. Patients who are expected to receive systemic pre/peri-operative corticosteroid therapy other than as anti-emetic prophylaxis 6. Patients receiving amisulpride for any indication within the 2 weeks prior to randomization 7. Patients known to be allergic to amisulpride or any of the excipients of amisulpride drug product; or to dexamethasone or ondansetron 8. Patients with a significant ongoing history of vestibular disease or dizziness 9. Patients being treated with regular anti-emetic therapy (dosed at least three times per week), which is still ongoing less than 1 week prior to screening 10. Patients being treated with levodopa, or any other dopamine D2-agonist 11. Patients who are pregnant or breast feeding 12. Patients with congenital long QT interval (QT) syndrome 13. Patients with a tumor of the anterior pituitary 14. Patients who have received emetogenic anti-cancer chemotherapy in the previous 4 weeks 15. Any other concurrent disease or illness that, in the opinion of the investigator makes the patient unsuitable for the study 16. Patients who have previously participated in this study or who have participated in another interventional clinical study involving pharmacological therapy within the previous 28 days (or longer exclusion period, if required by national or local regulations) 17. Where local laws/regulations require: patients under legal protection
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Evaluate Complete Response | 1 Day | Defined as no vomiting/retching (absence of PONV) and no use of anti-emetic rescue medication, during the first 24 hours after completion of surgery. Subjects will be questioned and assessed. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Use of rescue medication | 1 Day | Document use of rescue medication. |
| Occurrence and severity of post-operative nausea | 1 Day | An episode of nausea should be recorded any time that a subject spontaneously complains of nausea (including a request for rescue medication due to nausea). Subjects considered able to understand and provide a meaningful response should be asked if they have nausea (feel sick or other equivalent words) at the following times after completion of surgery (wound closure), unless an episode of PONV or discharge of the subject from the site has already occurred prior to the time point: 1 hour, 2 hours, 6 hours and 24 hours or when they first vomit, retch or receive rescue medication. In subjects aged ≥ 6 years, at the above time points and for any spontaneously reported nausea episode, nausea severity should be scored using the validated 6-point Baxter Retching Faces (BARF) scale. |
| Time to emergence of PONV | 1 Day | Observe for, question and document emergence of vomiting/retching and nausea. In subjects aged ≥ 6 years, at specified time points and for any spontaneously reported nausea episode, nausea severity should be scored using the validated 6-point Baxter Retching Faces (BARF) scale. |
| Time to emergence of vomiting/retching, significant nausea, and rescue medication, individually | 1 Day | Observe for emergence of vomiting/retching, determine significance of nausea, and note rescue medication, individually. |
| Occurrence of post-operative vomiting/retching | 1 Day | Subjects considered able to understand and provide a meaningful response should be asked if they have nausea (feel sick or other equivalent words) at the following times after completion of surgery (wound closure), unless an episode of PONV or discharge of the subject from the site has already occurred prior to the time point: 1 hour, 2 hours, 6 hours and 24 hours or when they first vomit, retch or receive rescue medication. In subjects aged ≥ 6 years, at the above time points and for any spontaneously reported nausea episode, nausea severity should be scored using the validated 6-point Baxter Retching Faces (BARF) scale. |
| The above variables in the sub-groups of patients who did and did not receive opioid analgesia | 1 Day | Concomitant medications will be reviewed. |
| Safety: The nature and frequency of adverse events and laboratory and electrocardiography (ECG) abnormalities | 7 Days | Adverse events, laboratory and ECG abnormalities will be noted. Blood samples should be drawn at screening (unless recent pre-existing results are available) and again post-operatively, as soon as practically possible after the patient's entry to the post-anesthesia care unit, recovery room or equivalent, and in any event within 1 hour after the end of surgery. Twelve-lead ECGs will be collected at screening. An ECG already taken as part of medical care within the period of 2 weeks prior to screening may be used to determine eligibility and to provide baseline ECG data. In the peri-/post-operative period, continuous Holter monitoring of the ECG will be performed, from at least 10 minutes prior until at least 2 hours after the start of administration of amisulpride study medication. |
| Key pharmacokinetics parameter - Peak Plasma Concentration | 1 Day | Plasma samples will be drawn as required at specified timepoints to determine the PK profile of peak plasma concentration of amisulpride in subjects. |
| Key pharmacokinetics parameter - Total Exposure | 1 Day | Plasma samples will be drawn as required at specified timepoints to determine the PK profile of total exposure of amisulpride in subjects. |
| Different variables during different time ranges after the end of surgery (0-2 h, 2-6 h and 6-24 h) | 1 Day | Subjects considered able to understand and provide a meaningful response should be asked if they have nausea (feel sick or other equivalent words) at the following times after completion of surgery (wound closure), unless an episode of PONV or discharge of the subject from the site has already occurred prior to the time point: 1 hour, 2 hours, 6 hours and 24 hours or when they first vomit, retch or receive rescue medication. In subjects aged ≥ 6 years, at the above time points and for any spontaneously reported nausea episode, nausea severity should be scored using the validated 6-point Baxter Retching Faces (BARF) scale. |
Countries
Canada, France, Germany, United States
Outcome results
None listed