Postoperative intestinal obstruction. Postoperative intestinal obstruction
Conditions
Interventions
Intervention 1: This study will be done on 90 women from the 22 December 2013 to 21 March 2014 at the Emam khomeini Hospital in Sari will be delivered by cesarean section .Intervention Group are cons
Treatment - Drugs
Placebo
This study will be done on 90 women from the 22 December 2013 to 21 March 2014 at the Emam khomeini Hospital in Sari will be delivered by cesarean section .Intervention Group are consisted of 45 case
Control group are consisted of 45 cases that drink 20 ml of the placebo in two half-hour interval, 6 hours after surgery. This group will be observed under the routine care after cesarean. Thus, their
Sponsors
Dr. Minaei; Vice chancellor for research Traditional Medicine Faculty of Tehran University of Medica
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: fasting for at least 8 hours before surgery; received a maximum of 4 doses of intravenous antibiotics; having a gestational age of 42-38 weeks; having good vital signs; no unusual complications of surgery; absence of fever before operation; lack of medical disorders and obstetric patients addicted to cigarettes and illegal drugs are not. Exclusion criteria: the patient withdrew from the study, those at risk for ileus and aspiration ( background radiation , anastomotic stricture , peptic ulcer, esophagitis, intestinal obstruction ), a lot of individuals taking sedatives, obstetric complications such as fatty liver of pregnancy, preeclampsia, diabetes, placental abruption, chorioamnionitis, post-operative complications ( atonic uterus, antibiotic therapy, more than four doses ), intraoperative complications ( severe adhesion, blood transfusion, injury to bowel and bladder ), personal discharge, during over 90 minutes, the use of magnesium sulfate for the possibility of nausea, infection, hypothyroidism, hyperparathyroidism, neuromuscular disease, excessive intestinal manipulation is obvious.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bowel sound. Timepoint: Each half-hour intervals , one hour after the intervention until the first sound will be heard. Method of measurement: Bowel sound auscultation by Stethoscope.;Flatus. Timepoint: First flatus. Method of measurement: Check list.;Defecation. Timepoint: The first defecation after caesarean. Method of measurement: Check list.;The time of discharge. Timepoint: At discharge. Method of measurement: Check list or file. | — |
Secondary
| Measure | Time frame |
|---|---|
| Bloat. Timepoint: Befor and after intervention. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyde Sedighe Yosefi
Traditional Medicine Faculty, Tehran University of Medical Sciences
Outcome results
None listed