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Pain Intensity AssessmentEANCT07041632

Pain Relief in Women Undergoing Oocyte Retrieval (OR) With Electro-acupuncture (EA) or Conscious Sedation (CS) in a Single Assisted Reproduction Centre.

A study testing electro-acupuncture and Conscious sedation in people with Pain Intensity Assessment, run by Singapore General Hospital at 1 site in Singapore.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study aims to determine whether one can replace pain relief in women undergoing oocyte retrieval (OR) using electro-acupuncture (EA) instead of conscious sedation (CS). Read more about this study

Who is it for?
Ages 21 to 45 years, women onlyHealthy volunteers can take part
Conditions the study is for
Pain Intensity Assessment
What is being tested?
electro-acupuncture and Conscious sedation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteSingapore
Study dates
Jan 2015to 31 Jan 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 to 45 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Inclusion Criteria: all women undergoing ivf and have given consent -

Exclusion Criteria: women who have infectious skin diseases, women who were unwilling to accept acupunture, history of bleeding disorders.

-

Trial locations and contacts

1 site in 1 country.

Singapore1 site
  • Centre for Assisted Reproduction

    Singapore, 165608

Other trials in Singapore

About this study

Official title: Can Acupuncture Replace Conscious Sedation in In-Vitro-Fertilization Transvginal Oocyte Retrievals?

This study aims to determine whether one can replace pain relief in women undergoing oocyte retrieval (OR) using electro-acupuncture (EA) instead of conscious sedation (CS).

Read the detailed description

A total of 60 women were randomized and 29 women were on electro-acupuncture (EA) versus 27 women on conscious sedation (CS) with intravenous medication for transvaginal egg extraction (OR) in IVF. Pain scores were recorded before , during and after egg extraction when the women were on conscious sedation and electro-acupuncture. Side effects were recorded. Physical parameters were recorded. Livebirth outcome were also recorded.

Being tested
electro-acupuncture, Conscious sedation
Keywords
acupuncture, oocyte retrieval, sedation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • electro-acupunctureOther

    electro-acupuncture for pain relief in egg collection in IVF

  • Conscious sedationOther

    IVf egg collection using conscious sedation as the usual analgesia

Study groups in NCT07041632
Study groupRoleWhat they receive
electro-acupunctureActive comparatorElectro-acupunture is compared to Conscious sedation during egg collection in IVF
Receives: Other: electro-acupuncture
Conscious sedation for egg collectionActive comparatorConscious sedation is the common analgesia used in egg collection in IVF
Receives: Other: Conscious sedation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain relief during egg collection

    Pain score 1 to 10 during egg collection in IVF compared between using acupuncture and conscious sedation

    Measured: from start of egg collection. to 120 minutes after egg collection

Secondary outcomes (1)
  1. Stress, satisfaction measurement and physical parameters between acupuncture and conscious sedation during egg collection in IVF

    Stress score and satisfaction outcome scores 0 to 10 for pain relief between acupuncture and conscious sedation during egg collection were recorded. For the stress score, zero is equivalent to no stress and 10 indicates the worst possible stress. For the satisfaction score, zero is equivalent to no satisfaction at all and 10 is the highest satisfaction.

    Measured: Up to 120 minutes after egg collection

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jun 2025
  2. Study startJan 2015
  3. Primary completion31 Dec 2017
  4. Study completion31 Jan 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
randomised control
Masking
None (open label)
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07041632
Sponsor's protocol ID
Acupuncture in IVF
Other IDs
TCMCRG3103002
Acronym
EA
Status last verified
Jun 2025
First submitted
19 May 2025
Last updated
27 Jun 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: This study has completed a few years ago.

Questions about this trial

What is this clinical trial studying?

A study testing electro-acupuncture and Conscious sedation in people with Pain Intensity Assessment, run by Singapore General Hospital at 1 site in Singapore.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Singapore. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain relief during egg collection (time frame: from start of egg collection. to 120 minutes after egg collection). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Jun 2025.

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