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The First ERAS Protocol for Cesarean Delivery in Serbia at the University Hospital

P

Pujic Borislava

Status

Unknown

Conditions

Cesarean Delivery

Treatments

Combination Product: ERAS protocol

Study type

Interventional

Funder types

Other

Identifiers

NCT04058444
0712960805046

Details and patient eligibility

About

This study is designed to help us with ERAS (Enhanced Recovery After Surgery) Protocol for Cesarean Delivery implementation with goal to improve patient satisfaction and decrease length of stay at hospital. This will improve patient treatment and decrease total hospital costs.

Full description

ERAS assumes cooperation between obstetricians, anesthesiologists and parturient. This is the new concept because patient have an active role in the whole process. Pregnant patient receives the first information about ERAS from obstetrician and anesthesiologist before the scheduled cesarean delivery. Patient condition optimization is necessary. Antibiotic prophylaxis, no bowel preparation and arriving to the hospital on the day of surgery are basic principles. All patients are done under spinal anesthesia. DVT (Deep Venous Thrombosis) prophylaxis starts postoperatively. Early mobilization, early oral intake and urinary catheter removal on the day of surgery with multimodal analgesia is mandatory.

Enrollment

200 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All healthy patients from 18-45 years for scheduled Cesarean Delivery

Exclusion criteria

  • Age younger then 18 years old and older then 45 years
  • Urgent and emergent Cesarean Delivery
  • Preeclampsia
  • Contraindications for spinal anesthesia
  • Abnormal placentation

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

ERAS Group
Experimental group
Description:
Perioperative management follows the ERAS (Enhanced Recovery After Surgery) protocol
Treatment:
Combination Product: ERAS protocol
Control Group
Experimental group
Description:
Perioperative management follows the conventional program
Treatment:
Combination Product: ERAS protocol

Trial contacts and locations

1

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Central trial contact

Borislava Pujic, PhD; Lidija Jovanovic, MD

Data sourced from clinicaltrials.gov

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