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pain control and satisfaction patients undergoing colonoscopy

Comparison among four metods of medication administration on pain control and satisfaction patients undergoing colonoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015112221806N2
Enrollment
164
Registered
2016-03-12
Start date
2015-12-22
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. Pain localized to other parts of lower abdomen

Interventions

Intervention 1: In the group A used of drugs (midazolam + fentanyl) 2 mg/kg bolus intravenous fentanyl and midazolam 0.03 mg/kg as a bolus. Intervention 2: In the group B is used the drug (hydroxyzine
Treatment - Drugs
In the group A used of drugs (midazolam + fentanyl) 2 mg/kg bolus intravenous fentanyl and midazolam 0.03 mg/kg as a bolus.
In the group B is used the drug (hydroxyzine + fentanyl) so that consumed two hours before colonoscopy, two tablets of 25 mg hydroxyzine and fentanyl 2 mg / kg intravenous bolus.
In the group C is injected intravenously drugs (ketorolac) so that 30 minutes before the colonoscopy 0.5mg / kg.
In the group D is injected intravenously drugs (ketorolac+ fentanyl) so that bolus intravenous fentanyl of 2 mg/kg, 30 minutes before the colonoscopy ketorolac 0.5 mg/kg.

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria :Non urgency of colonoscopy?At least 18 years of age for participant?Patient satisfaction?The lack of acute gastrointestinal bleeding?The patient is placed first under colonoscopy. Exclusion criteria:If the patient needs more medication at colonoscopy time?Sensitivity to patients' medication.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain patients-Patient satisfaction. Timepoint: 6 months. Method of measurement: standard questionnaires VAS and GHAA- 9.;Patients' satisfaction. Timepoint: 6 months. Method of measurement: standard questionnaires VAS and GHAA- 9.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Dabiri

Semnan University of Medical Sciences

dabirirzf@yahoo.com+98 23 3343 7821

Outcome results

None listed

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