Cesarean Section Clinical Trial
— MLCOfficial title:
French Ambulatory and Misgav Ladach Cesarean Section Techniques : a Results of a Comparative Randomized Trial.
Verified date | December 2020 |
Source | University Tunis El Manar |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In the last decades cesarean section rates are getting higher in many countries. The rise in those rates encourages obstetricians to improve operative techniques for a better maternal and fetal outcome. Despite its worldwide spread, a general consensus on the most appropriate technique to use has not yet been reached. The most known surgical technique is the MLC . A modified extraperitoneal method of caesarean section :" French Ambulatory Cesarean Section ( FAUCS) was described in the middle of the 90's by "Denis Fauck" and "Jacques Henri Ravina " However, no study comparing these two cesarean techniques was conducted. From where the investigators initiate this study .
Status | Completed |
Enrollment | 100 |
Est. completion date | April 30, 2019 |
Est. primary completion date | March 20, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 48 Years |
Eligibility | Inclusion Criteria: - Singleton pregnancy - gestational age of at least 37 weeks of amenorrhea - indication of elective cesarean delivery mode (breech presentation ; Fetal macrosomia ; Placenta previa) Exclusion Criteria: - Fetal pathology diagnosed prenatally( intrauterine growth restriction , malformation, genetic pathology ... ) - Morbidity adherent placenta - emergency Cesarean section |
Country | Name | City | State |
---|---|---|---|
Tunisia | Kaouther Dimassi | Tunis | Sidi Daoued La Marsa |
Lead Sponsor | Collaborator |
---|---|
University Tunis El Manar |
Tunisia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | changes in post operative pain | changes in postoperative analgesic requirements, changes in self reported pain using the Visual Analog Scale for Pain (VAS Pain) intensity ( The pain VAS is a single-item scale.For pain intensity, the scale is most commonly anchored by "no pain" (score of 0) and "pain as bad as it could be" or "worst imaginable pain" (score of 100 [100-mm scale] ) | 6 hours ; 12 hours , 18 hours , 24 hours | |
Primary | delay to hospital discharge | report of total days spent in hospital after surgery | up to 72 hours | |
Secondary | blood loss | change in hemoglobin and hematocrit rate | the day before surgery and the day after surgery (24 hours) | |
Secondary | operation time | total operation time ; time to fetal extraction ; time to uterine sutures | during the surgery | |
Secondary | rate of short term incidents | rate of hemorrhage, rate of transfusion, rate of bladder injury | during the surgery and 24 hours after surgery | |
Secondary | patient autonomy questionnaire | time to first spontaneous miction, time to stand up ; time to first complete meal, time to first breastfeeding | up to 48 hours after surgery | |
Secondary | newborn overall condition | Apgar score ( The Apgar score is determined by evaluating the newborn baby on five simple criteria on a scale from zero to two, then summing up the five values thus obtained. The resulting Apgar score ranges from zero to 10. The five criteria are summarized using words chosen to form an ackronym (Appearance, Pulse, Grimace, Activity, Respiration).he test is generally done at 1 and 5 minutes after birth and may be repeated later if the score is and remains low. Scores 7 and above are generally normal; 4 to 6, fairly low; and 3 and below are generally regarded as critically low and cause for immediate resuscitative efforts.) | 5 minutes from birth | |
Secondary | neonatal acid base balance | Cord blood gases | immediately after fetal extraction |
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