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To relieve crisis pain in sickle cell anemia patients

A clinical trial to comparison the effectiveness of injection ketorolac with injection morphine to relieve the crisis pain in sickle cell anemia patients.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016072511956N6
Enrollment
84
Registered
2017-05-10
Start date
2017-02-19
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

Sickle cell anemia. Sickle-cell anaemia with crisis

Interventions

Intervention 1: Intervention group I: Patients with sickle cell anemia are receiving 30 mg injection ketorolac. Pain reliefs will assessment based on the visual analog scale before and 5 minutes after
Treatment - Drugs
Intervention group I: Patients with sickle cell anemia are receiving 30 mg injection ketorolac. Pain reliefs will assessment based on the visual analog scale before and 5 minutes after intervention.
Intervention group II: Patients with sickle cell anemia are receiving 4-10 mg injection morphine at 4 to 5 ml injection water solution. Pain reliefs will assessment based on the visual analog scale be

Sponsors

Vice Chancellor for Research, Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: use of studying medicine; no prior history of cardiovascular and respiratory diseases; not having hypertension; not using other analgesic drug. Exclusion criteria: unwillingness to continue the study; major side-effects due to the use of medications; addicted, especially for morphine injection; having sensitivity.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain relief. Timepoint: Before and 5 minutes after intervention. Method of measurement: The visual analog scale.

Secondary

MeasureTime frame
Side-effects of medications (nausea and vomiting, dizziness, respiratory depression, skin rash in the area of injection, menorrhagia after injection, hypotension, seizures, drowsiness, allergic reactions, etc). Timepoint: 5 minutes after intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomaye Sadat Hosseiny

Mashhad University of Medical Sciences

somaye_2004a@yahoo.com+98 51 3731 7147

Outcome results

None listed

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