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Study of anti-nausea drug metoclopramide easily nasogastric tube insertion compared with patients not receiving.

Efficacy of pre-emptive metoclopramide on patients' pain, discomfort and nausea associated with NG Tube insertion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015083023696N2
Enrollment
46
Registered
2015-12-23
Start date
2014-04-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pain, discomfort and nausea associated with NG Tube insertion. Complications of action on the digestive system

Interventions

Intervention 1: Intervention group, before planting NG tube, 10 mg metoclopramide (manufacturing pharmaceutical company Al-Hawi) will be given intravenously 15 minutes before the procedure. The pipeli
Treatment - Drugs
Intervention group, before planting NG tube, 10 mg metoclopramide (manufacturing pharmaceutical company Al-Hawi) will be given intravenously 15 minutes before the procedure. The pipeline project done
control group, with a similar volume of saline (as a placebo) will be administered.The pipeline project done by students trained and at zero, 30 and 60 minutes on the completed list .

Sponsors

Mazandaran University Of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: inclusion criteria:patient's willingness to participate in the study and obtain informed consent; Indications put nasogastric tube; Age over 18 years. exclusion criteria:Lack of patient awareness; Patients with unstable hemodynamic status; Having nosebleeds during the study period; Having problems anatomical nose; Trauma patients; Hypersensitivity to metoclopramide; Medications interact with metoclopramide; Pregnancy;patients with nausea and vomiting will ; If more than two attempts for nasogastric tube insertion is done.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Discomfort during intubation. Timepoint: Zero minutes, 30 minutes, 60 minutes. Method of measurement: score pain, nausea, discomfort.;Nausea and vomiting. Timepoint: Zero minutes, 30 minutes, 60 minutes. Method of measurement: score pain, nausea, discomfort.;Pain. Timepoint: Zero minutes, 30 minutes, 60 minutes. Method of measurement: score pain, nausea, discomfort.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Hajizadeh

Mazandaran Univercity Of Medical Science

mhoseininejad@mazums.ac.ir+1 133377169

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026