| dc.contributor.author | Abbasinazari, Mohammad | en_US | 
| dc.contributor.author | Panahi, Yunes | en_US | 
| dc.contributor.author | Mortazavi, Seyed Alireza | en_US | 
| dc.contributor.author | Fahimi, Fanak | en_US | 
| dc.contributor.author | Azizian, Homa | en_US | 
| dc.contributor.author | Mohtashami, Saiid | en_US | 
| dc.contributor.author | Poorhoseingholi, Mohammad amin | en_US | 
| dc.contributor.author | bakhtiari, kambiz | en_US | 
| dc.date.accessioned | 1399-07-09T06:59:37Z | fa_IR | 
| dc.date.accessioned | 2020-09-30T06:59:37Z |  | 
| dc.date.available | 1399-07-09T06:59:37Z | fa_IR | 
| dc.date.available | 2020-09-30T06:59:37Z |  | 
| dc.date.issued | 2014-10-01 | en_US | 
| dc.date.issued | 1393-07-09 | fa_IR | 
| dc.date.submitted | 2014-01-11 | en_US | 
| dc.date.submitted | 1392-10-21 | fa_IR | 
| dc.identifier.citation | Abbasinazari, Mohammad, Panahi, Yunes, Mortazavi, Seyed Alireza, Fahimi, Fanak, Azizian, Homa, Mohtashami, Saiid, Poorhoseingholi, Mohammad amin, bakhtiari, kambiz. (2014). Effect of a Combination of Omeprazole Plus Sustained Release Baclofen Versus Omeprazole Alone on Symptoms of Patients with Gastroesophageal Reflux Disease (GERD). Iranian Journal of Pharmaceutical Research, 13(4), 1221-1226. doi: 10.22037/ijpr.2014.1593 | en_US | 
| dc.identifier.issn | 1735-0328 |  | 
| dc.identifier.issn | 1726-6890 |  | 
| dc.identifier.uri | https://dx.doi.org/10.22037/ijpr.2014.1593 |  | 
| dc.identifier.uri | http://ijpr.sbmu.ac.ir/article_1593.html |  | 
| dc.identifier.uri | https://iranjournals.nlai.ir/handle/123456789/313423 |  | 
| dc.description.abstract | Previous studies have reported the efficacy of baclofen in the treatment of Gastroesophageal Reflux Diseases (GERD). The objective of present study is to evaluate the effect of co-administration of omeprazole 20 mg/d plus sustained Release baclofen (SR baclofen) vs omeprazole 20 mg/d plus placebo on alleviation of symptoms in patients with a diagnosis of GERD. A prospective, double blind, placebo controlled trial included 50 patients with diagnosis of GERD have been done. Patients were randomly selected to receive either SR baclofen or a placebo in addition to omeprazole 20 mg/d for a period of 2 weeks. Patients were questioned regarding heartburn, regurgitation, chest pain and hoarseness at the base line and after 2 weeks. All patients tolerated the medications and no patients failed to complete the study due to adverse drug reactions. A total of 53 patients completed the study, 25 in SR baclofen and 28 in placebo group. After 2 weeks, 1 patient (4%) in SR baclofen group reported heartburn and regurgitation. However 13(46.4%) and 15 (53.6%) of patients in the placebo group had heartburn and regurgitation respectively. The analysis of the data shows that there is a significant difference between the two groups in heartburn and regurgitation (p < 0.0001, p < 0.0001 respectively). Statistical analysis revealed a significant difference in two groups regarding total GERD score (p | en_US | 
| dc.format.extent | 527 |  | 
| dc.format.mimetype | application/pdf |  | 
| dc.language | English |  | 
| dc.language.iso | en_US |  | 
| dc.publisher | School of Pharmacy, Shahid Beheshti University of Medical Sciences | en_US | 
| dc.relation.ispartof | Iranian Journal of Pharmaceutical Research | en_US | 
| dc.relation.isversionof | https://dx.doi.org/10.22037/ijpr.2014.1593 |  | 
| dc.subject | Baclofen | en_US | 
| dc.subject | Omeprazole | en_US | 
| dc.subject | GERD | en_US | 
| dc.subject | sustained release | en_US | 
| dc.subject | Pharmacotherapy (Clinical Pharmacy) | en_US | 
| dc.title | Effect of a Combination of Omeprazole Plus Sustained Release Baclofen Versus Omeprazole Alone on Symptoms of Patients with Gastroesophageal Reflux Disease (GERD) | en_US | 
| dc.type | Text | en_US | 
| dc.type | Research article | en_US | 
| dc.contributor.department | shahid Beheshti University of Medical Sciences | en_US | 
| dc.contributor.department | Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences | en_US | 
| dc.contributor.department | Shahid Beheshti University of Medical Sciences | en_US | 
| dc.contributor.department | Department of clinical pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran | en_US | 
| dc.contributor.department | Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences | en_US | 
| dc.contributor.department | Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences | en_US | 
| dc.contributor.department | Shahid Beheshti University of Medical Sciences | en_US | 
| dc.contributor.department | Shahid Beheshti University of Medical Sciences | en_US | 
| dc.citation.volume | 13 |  | 
| dc.citation.issue | 4 |  | 
| dc.citation.spage | 1221 |  | 
| dc.citation.epage | 1226 |  | 
| nlai.contributor.orcid | 0000-0003-4194-1846 |  |