A Study of Intravenous (IV) Amisulpride for Prophylaxis of Post-operative Nausea and Vomiting (PONV) in Pediatric Patients

• Status: Not yet recruiting
• Trial end date: 2024-12-30
• Target enrollment: 0
• Participant gender: All

Summary

Randomized, double-blind, pediatric trial of amisulpride for prophylaxis of post operative nausea and vomiting

• Phase: Phase 2/Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Acacia Pharma Ltd
• Collaborators: Amicus CD LLC; Premier Research Group plc
• Treatments: Amisulpride; Dexamethasone; Ondansetron

Criteria

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 International Conference on Harmonization (ICH) M3 guidance, e.g., abstinence from sexual intercourse, surgical sterilization (of subject or partner), combined oral contraceptive pill, a double-barrier method of contraception such as either an intra-uterine device (IUD) or an occlusive cap with spermicide, in conjunction with partner's use of a condom, 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

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