A Research Comparing Efficacy of PIEB Plus PCEA vs CEI Plus PCEA for Labour Analgesia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorAiman Bin Ab Adzim

About this trial

During labour process, one of the most effective ways to manage pain is via epidural analgesia. It is commonly and widely use for all pregnant women underwent labour process. It provides good pain relief during labour process especially for contraction pain and pain during descending of baby during delivery.

During epidural insertion, a small catheter (which is flexible and thin) will be inserted via epidural needle at the back. Using this epidural catheter, pain medication will be given to ease and help controlling the pain. This procedure is usually done after you have been admitted to labour room.

In this research, investigator will compare among two different method of epidural administration which are:

\- Programmed Intermittent Epidural Bolus with Patient-Controlled Epidural Analgesia (PIEB +

PCEA):

* This method will enable the medication to be served automatically within the set time through the epidural catheter and allows for participants to manage additional boluses of medication according to the participants pain level.

\- Continuous Epidural Infusion with Patient-Controlled Epidural Analgesia (CEI + PCEA): * This method will deliver continuous infusion of medication and allows for participants to manage additional boluses of medication according to the participants pain level.

Investigator want to determine the best method between this two in order to have better pain control, less usage of medication and improving the satisfaction of patient. In participating this research, the participants will help us in understanding the best method to be use for the labour process in which eventually help other future patient who is in need.

Eligibility criteria

Qualifiers

All pregnant female > 36 weeks of gestation

Age 18 years old and above

ASA I and II

Consented for study

Disqualifiers

Allergies to LA and opioids

Severe systemic and mental disease

Contraindication to regional analgesia

Hemodynamic instabilities

Trial design

Treatments tested in this trial

  • Programmed intermittent epidural bolus 10 ml
  • continuous epidural infusion

Treatment groups

88 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Aiman Bin Ab Adzim

Lead sponsor

Universiti Putra Malaysia

Sponsor institution