Observation of Respiration Following Regional Anaesthesia With Intrathecal Opioids for Caesarean Section

This study has been completed.
Information provided by:
NHS Greater Clyde and Glasgow
ClinicalTrials.gov Identifier:
First received: October 12, 2007
Last updated: February 3, 2009
Last verified: February 2009
Spinal Administration of opioids offers segmental analgesia, but has side effects including pruritus, nausea and vomiting, urinary retention, hypotension, and respiratory depression, both early and delayed. Many Centres in the UK now routinely use supplementation of spinal anaesthesia from bupivacaine with intrathecal fentanyl or diamorphine. If Fentanyl is used, this is usually accompanied by connection to a i.v. Morphine patient-controlled analgesia (PCA)-device in the postoperative period, whereas the use of intrathecal diamorphine seems to result in a reduction in post-operative morphine requirements, which has obviated the need for PCA devices in many centres. There has been recent controversy over which opioid is safer to use with regards to the risk of respiratory depression.1,2 The investigators want to investigate, whether intrathecal diamorphine causes less or more post-operative respiratory depression in healthy mothers undergoing elective caesarean section than intrathecal fentanyl plus post-operative morphine PCA.

Respiratory Depression

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Observation of Respiration Following Regional Anaesthesia With Intrathecal Opioids: a Comparison Between Diamorphine and Fentanyl Combined With Postoperative Morphine PCA Using a Carbon Dioxide Tension and Pulse Oximetry Sensor (TOSCA)

Resource links provided by NLM:

Further study details as provided by NHS Greater Clyde and Glasgow:

Primary Outcome Measures:
  • transcutaneous carbon dioxide tension [ Time Frame: within the first 24 hours after surgery ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • oxygen-saturation, respiratory rate, neurological status, need for administration of naloxone and/or active airway management [ Time Frame: within first 24 hours after surgery ] [ Designated as safety issue: Yes ]

Enrollment: 90
Study Start Date: October 2007
Study Completion Date: July 2008
Primary Completion Date: July 2008 (Final data collection date for primary outcome measure)
D, F

Group D will be patients at Princess Royal Maternity Hospital in Glasgow, where supplementation with intrathecal diamorphine 300mcg is the current anaesthetic technique of choice.

Group F will be patients at the Queen Mother's Maternity Hospital in Glasgow, where supplementation with intrathecal fentanyl 15mcg plus post-operative morphine PCA is the current anaesthetic technique of choice for elective caesarean section.

  Show Detailed Description


Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Elective caesarean section Healthy pregnant women

Inclusion Criteria:

  • 1st patient on list
  • ASA I or II
  • BMI <40 at booking
  • Term pregnancy +/- 2 weeks gestation

Exclusion Criteria:

  • ASA>II
  • BMI>40 at booking
  • History of Obstructive Sleep Apnoea (OSA)
  • Need for supplementation with intravenous Opioids intraoperatively
  • Conversion to GA
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00544947

United Kingdom
Princess Royal Maternity Hospital
Glasgow, United Kingdom, G4 0SF
Sponsors and Collaborators
NHS Greater Clyde and Glasgow
Principal Investigator: Stephan Dalchow, FRCA National Health Service
  More Information

Responsible Party: Dr Stephan Dalchow, NHS Greater Clyde&Glasgow
ClinicalTrials.gov Identifier: NCT00544947     History of Changes
Other Study ID Numbers: 07/S0704/67 
Study First Received: October 12, 2007
Last Updated: February 3, 2009
Health Authority: United Kingdom: Research Ethics Committee

Keywords provided by NHS Greater Clyde and Glasgow:
Respiratory Depression
Caesarean Section

Additional relevant MeSH terms:
Respiratory Insufficiency
Respiration Disorders
Respiratory Tract Diseases

ClinicalTrials.gov processed this record on May 24, 2016