Study to find out the effect of Camylofin 50 mg and Paracetamol 325mg drug in patients with acute colicky abdominal pai

Not Applicable

Conditions: Health Condition 1: K318- Other specified diseases of stomach and duodenum

Registration Number: CTRI/2024/01/061405

Lead Sponsor: Abbott Healthcare Pvt Ltd

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Closed to Recruitment of Participants

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

Female subjects aged 18 65 years

Patients attending OPD with acute colicky abdominal pain and having at least one episode of colicky pain within 24 hours prior to the visit

Non complicated cases of acute colicky abdominal pain may be confirmed by imaging tests such as Ultrasound Sonography USG performed prior to the treatment initiation to ensure no

complicated cases get recruited as perwill be performed at the discretion of the investigator

Patient willing to provide written informed consent to will be enrolled in the study

Exclusion Criteria

Patients with history of hypersensitivity to the study drugs any of study drugs ingredients

Patients who had undergone coronary artery bypass graft surgery with epilepsy or inflammatory bowel disease will be excluded

Patients with chronic abdominal pain such as Celiac disease lactose intolerance ulcerative colitis and Crohns disease

Patients who may have narrow angle glaucoma mechanical stenosis Pregnancy and lactation Urinary retention Mega colon GI

hemorrhage Tachyarrhythmia Porphyria

Patients with any other conditions or diseases that investigator considers as ineligible to enroll in the study based on approved

prescribing information

Study & Design

Study Type: Observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Percentage change in the mean intensity of pain based on the 100mm VAS score from baseline to EOSTimepoint: Percentage change in the mean intensity of pain based on the 100mm VAS score from baseline to EOS

Secondary Outcome Measures

Name	Time	Method
To assess how much time it takes on average for people to feel relief from pain by looking at a ten point reduction in the pain intensity score on the visual analogue scaleTimepoint: To assess how much time it takes on average for people to feel relief from pain by looking at a ten point reduction in the pain intensity score on the visual analogue scale