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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04461093
Other study ID # PalanosetronUSM
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 6, 2020
Est. completion date November 1, 2021

Study information

Verified date April 2024
Source Universiti Sains Malaysia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Postoperative nausea and vomiting (PONV) is defined as nausea and/or vomiting occurring within 24 hours after surgery, it commonly affects 20-30% patients but as high as 70-80% patients who are deemed high risk for PONV may be affected. PONV may cause unpleasant complications such as dehydration, electrolyte imbalance, suture dehiscence, aspiration of gastric contents, delayed recovery and prolonged hospital stay. Standard guideline recommended combination of anti-emetics to prevent PONV in high risk patients. The commonly used agents are dexamethasone and ondansetron which are cheaper although they are proven to be less effective as single agent when compared with newer agent such as palonosetron. As an adjunct or alternative to pharmacological treatment, acupressure P6 point has gained increasing attention for its possible value in preventing PONV. It is proven that acupressure reduced the incidences of PONV when combined with pharmacological treatment. It is postulated that acupressure active Aβ and Aδ fibres and stimulate the release of β-endorphine from hypothalamus. In addition, it is believed that acupressure might act on dopaminergic, serotonergic and norepinerphrinergic fibres which might has a role in PONV prevention.


Description:

This study is designed to compare the efficacy of palonosetron monotherapy versus combination of acupressure P6 point with dexamethasone and ondansetron in preventing PONV. It has been proven that palonosetron is more superior as single agent when compared with acupressure, dexamethasone and ondansetron separately. However, this might not be cost effective as palonosetron is more expensive than the other agents. In addition, the combination therapy has been reported better in preventing PONV when compared with monotherapy. The investigators need to investigate whether the combination of acupressure with dexamethasone and ondansetron exert an effect equal or even better than palonosetron monotherapy. The investigators hypothesis is the combination of acupressure P6 point with dexamethasone and ondansetron provide better prophylaxis againts PONV when compared with palonosetron. The requirement for rescue anti-emetics for combination of acupressure P6 point with dexamethasone and ondansetron group is lesser than palonosetron.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date November 1, 2021
Est. primary completion date November 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. ASA I or II female patients aged 18 - 65 years old in view female patients are at higher risk of postoperative nausea and vomiting. 2. Patients undergoing laparoscopic surgery. 3. High risk for PONV (APFEL score 3-4). Exclusion Criteria: 1. Patients with known allergic to dexamethasone, ondansetron and wristband. 2. Patients who take anti-emetic, emetogenic drugs and glucocorticoids within 24 hours before surgery. 3. Patients with upper limb disability which affect the application of wristband. 4. Obese patients with BMI > 35 in view acupressure P6 wristband might be too tight to fit patient's wrist which might affect the correct placement of pressure point. 5. Pre-existing vertigo

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Acupressure wristband and Palanosetron
Group 1 Patients with odd numbers labelled form will be Group I patients. They will receive intravenous dexamethasone 8mg during induction. Acupressure P6 wristband is applied after induction and removed prior to emergence to maintain blinding. Intravenous ondansetron 4mg is given prior to skin closure. Group 11 Patients with even numbers labelled form will be Group II patients who will receive intravenous palonosetron 0.075mg during induction.

Locations

Country Name City State
Malaysia Mohd Zulfakar Mazlan Kota Bharu Kelantan
Malaysia Mohd Zulfakar Mazlan, MBBS Kota Bharu Kelantan

Sponsors (1)

Lead Sponsor Collaborator
Mohd Zulfakar Mazlan, MBBS

Country where clinical trial is conducted

Malaysia, 

Outcome

Type Measure Description Time frame Safety issue
Primary The incidence of postoperative nausea and vomiting immediately, at Hours 6, postoperative.
Primary The incidence of postoperative nausea and vomiting immediately, at Hours 12, postoperative
Primary The incidence of postoperative nausea and vomiting immediately, at Hours 24, postoperative
Primary The incidence of postoperative nausea and vomiting immediately, at Hours 48, postoperative
Secondary The proportion of patients require rescue anti-emetics immediately, at Hours 6, postoperative.
Secondary The proportion of patients require rescue anti-emetics immediately, Hours 12, postoperative.
Secondary The proportion of patients require rescue anti-emetics immediately, Hours 24, postoperative.
Secondary The proportion of patients require rescue anti-emetics immediately, Hours 48, postoperative.
See also
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Completed NCT02809378 - The Effects of Anesthetic Techniques and Palonosetron Administration on the Incidence of PONV Phase 4
Completed NCT01650961 - The Effect of Palonosetron on the QTc Interval During Perioperative Period N/A