Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:12 AM
Ignite Modification Date:
2025-12-25 @ 4:12 AM
NCT ID:
NCT02777320
Eligibility Criteria:
Inclusion Criteria:
* Patients who presented with complaints of leg pain radiating the sciatic nerve tracings to the emergency services (Which may or may not be accompanied back pain),
* Positive Laseque test identified patients in physical examination,
* Patients whose complaints have started in the last week,
* Younger than 21 years old,
* Older than 65 years old.
Exclusion Criteria:
* Patients who have a leg or low back pain longer than a week Have a direct blunt trauma to the legs or lumbar area in the last week,
* Pretreatment linear 100-mm visual analog scale (VAS) pain score less than 40 mm,
* Patients who have drop foot, paralysis and other neurological symptoms in physical examination.
* Patients with blood pressure less than 90mmHg in the arrival of emergency services.
* Patients with malignancy, cauda equina syndrome, ankylosing spondylitis, rheumatoid arthritis or inflammatory arthritis contain any of the disease in his/her CV.
* Patients with any history of chronic pain syndrome.
* Patients who receive pain killers, antidepressants, anticonvulsants, muscle relaxants, steroids within 6 hours before the ED visit,
* Patients with a history of Substance Dependence or alcohol abuse
* Patients had a fever (\>37.9)
* Allergy or previous adverse reaction to the studied drugs(Ibuprofen, Paracetamol), received agents to inhibit the secretion of acid (PPIs or histamine-2 receptor antagonists), antispasmodics, or nonsteroidal anti-inflammatory drugs
* were pregnant or breast-feeding,
* inability to comprehend the VAS evaluation,
* or refused to participate in the study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
21 Years
Maximum Age:
65 Years
Study:
NCT02777320
Study Brief:
Protocol Section:
NCT02777320