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Acupuncture for Prevention of Itch in Caesarean Section

Acupuncture for the Prevention of Intrathecal Diamorphine-induced Itch in Elective Caesarean Section: A Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03458572
Enrollment
80
Registered
2018-03-08
Start date
2018-02-12
Completion date
2018-11-15
Last updated
2025-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pruritus

Keywords

Caesarean section

Brief summary

This study aims to determine the effectiveness of using a commercially available acupuncture stud at the LI11 acupuncture point at reducing the severity of itch caused by intrathecal diamorphine in elective caesarean section.

Detailed description

Itch is a very common complication of diamorphine used in spinal anaesthesia for caesarean section with a local incidence of 78%. It ranges from irritating to distressing and difficult to treat and can adversely affect maternal satisfaction, wellbeing and bonding with their baby. This trial aims to determine whether acupuncture using a commercially-available acupuncture stud at the LI11 point reduces the incidence and severity of post-operative itching in patients undergoing elective caesarean section under spinal anaesthesia with intrathecal diamorphine. 80 women having a planned caesarean section under spinal anaesthesia will be recruited by informed consent and randomised to the intervention group or the control group. The intervention group will receive an acupuncture stud at the LI11 point on either arm and the control group will receive acupuncture with a similar stud containing a smaller needle at a non-acupuncture point on either arm. The stud can be left in-situ until the followup visit the following morning or removed earlier at the participants discretion. All other care will be the usual clinical care including access to anti-itching drugs as required. Participants will be visited by a member of the research team at 3-5 hours following the start of their spinal anaesthetic and asked to mark their itch on an 11 point visual analogue scale (VAS). They will also be visited by a member of the research team the following morning, asked to rate their worst itch on the same scale and asked how troublesome they have found their itch (none, mild, moderate, severe). The administration of any anti-itch drugs will be recorded and if the acupuncture stud has not been removed it will be removed at this time. If effective, acupuncture with an acupuncture stud would provide an acceptable, convenient, safe and cost-effective treatment.

Interventions

DEVICESeirin Pyonex press needle acupuncture

Acupuncture

Sponsors

Obstetric Anaesthetists' Association United Kingdom
CollaboratorOTHER
Sheffield Teaching Hospitals NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* ASA1-3 patients with uncomplicated pregnancies undergoing elective caesarean section with a plan for spinal anaesthesia with intrathecal diamorphine.

Exclusion criteria

* Age under 18. * Pre-existing itch or conditions associated with itch (eg cholestasis of pregnancy). * Pre-existing use of H1 receptor antagonists, non-selective antihistamines or ursodeoxycholic acid. * Severe perioperative complication or fetal death. * Conversion to general anaesthesia. * Unable to understand written and spoken English.

Design outcomes

Primary

MeasureTime frameDescription
Presence or absence of itchbetween 3 and 5 hours post injection of spinal anaestheticPresence or absence of itch

Secondary

MeasureTime frameDescription
Severity of itch on 11 point VAS scalebetween 3 and 5 hours post injection of spinal anaestheticSeverity of itch on 11 point VAS scale
Severity of worst overall itch on 11 point VAS scaleAt a follow up visit the next day following the spinal anaestheticSeverity of worst overall itch on 11 point VAS scale

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026