Pelvic PainPEARLNCT07305025
Pelvic Pain Electro-Acupuncture
A study testing Electro acupuncture in people with Pelvic Pain and Endometriosis, run by St. Olavs Hospital at 1 site in Norway.
Trial summary
The aim of the study is to investigate if a series of up to 9 treatment sessions of electroacupuncture can be used to alleviate pain in women with suspected endometriosis, scheduled for diagnostic laparoscopy Read more about this study
- Who is it for?
- Ages 18 to 45 years, women only
- Conditions the study is for
- Pelvic Pain, Endometriosis
- What is being tested?
- Electro acupuncture
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 38 participants
- Where
- 1 siteNorway
- Study dates
- 16 Dec 2025to 30 Apr 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 18 to 45 years
- Women only
- No healthy volunteers
- Adult
Who may be able to join
- Women aged 18-45 years referred for diagnostic laparoscopy with suspicion of endometriosis
- Experiencing moderate to severe pelvic pain
- Willing to commit to the treatment schedule and follow-up
- Understanding Norwegian or English to be able to communicate and fill out questionnaires
Who cannot join
- Pregnancy
- Use of opioid pain relief
- Concurrent participation in other pain management trials
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Norway1 site, 1 recruiting
- Recruiting
St Olav's University Hospital
Trondheim, 7006
Ingrid Volløyhaug
About this study
Official title: Pelvic Pain Electro-Acupuncture: Randomized Study for Symptom Liberation
The aim of the study is to investigate if a series of up to 9 treatment sessions of electroacupuncture can be used to alleviate pain in women with suspected endometriosis, scheduled for diagnostic laparoscopy
Read the detailed description
- Introduction Background: Endometriosis is a chronic inflammatory condition associated with significant pelvic pain, often requiring medical intervention. Globally, it is estimated that approximately 10 percent of reproductive-age females have endometriosis (1). Up to 70% of adolescent and adult females presenting for evaluation of chronic pelvic pain are diagnosed with endometriosis. While surgery and hormonal therapy are standard treatments, they may not be suitable or readily available for all patients. In addition, surgery is expensive and carries risk of complications. A systematic review and meta-analysis from 2023 including 331 women from six studies showed that acupuncture reduced overall pelvic pain and menstrual pain, but the evidence was low to moderate (2). The studies were non homogeneous regarding acupuncture style (Traditional Chinese, Japanese, ear acupuncture or unspecified), number of needles and duration of treatment. Another review from 2024 included 11 studies from China and three from other countries using different acupuncture techniques (3). They conclude that acupuncture is effective in alleviating dysmenorrhea and pelvic pain but the current evidence is limited and research focusing on subtypes of acupuncture is needed (3). Electro-acupuncture (EA) has been suggested as a promising approach to modulating pain perception and reducing inflammation. By influencing endogenous opioid release, regulating inflammatory cytokines, and improving pelvic blood flow, EA may provide effective symptom relief (4, 5). EA was more effective than conventional acupuncture in treating endometriosis related pain in a few studies (3, 6). Most previous studies are from China, and feasibility studies regarding type of acupuncture, duration of treatment, how women tolerate intervention and results on pelvic pain in a European setting are needed. Given the need for additional management options, particularly for women awaiting surgery or seeking alternatives to hormonal treatments, EA could offer valuable support in symptom relief. Aim: Primary aim: To assess the effect of acupuncture on pelvic pain in women with suspected endometriosis. Secondary aims: To assess the effect of acupuncture on pelvic floor muscle function, sexual function, quality of life. To determine feasibility for a larger-scale study.
- Study Design Type: Randomized Controlled Trial, Pilot study, non-blinded. Sample Size: 36 women with suspected endometriosis randomized to either acupuncture treatment or standard care. Women in the acupuncture group (n=18) will receive treatment in separate 3-week periods/blocks. Duration: Three weeks of acupuncture treatment with follow-up at end of treatment and 2-3 months post-treatment (day of surgery).
- Inclusion \& Exclusion Criteria Inclusion Criteria: Women aged 18-45 years referred for diagnostic laparoscopy with suspicion of endometriosis Experiencing moderate to severe pelvic pain Willing to commit to the treatment schedule and follow-up Understanding Norwegian or English to be able to communicate and fill out questionnaires Exclusion Criteria: Pregnancy Use of opioid pain relief Concurrent participation in other pain management trials.
- Intervention Rationale for point selection: Traditional Chinese Medicine (TCM) approaches treatment based on pattern differentiation, where diagnosis is guided by symptom presentation and observable signs. TCM recognizes multiple patterns for conditions like endometriosis, typically six distinct patterns. A key concept in TCM related to endometriosis is "qi and blood stagnation," a term that describes symptoms such as distension or sharp pain. While all cases of endometriosis in TCM include aspects of this pattern, the underlying TCM causes may vary. This protocol is designed to address the clinical presentation associated with qi and blood stagnation, making it standardized and broadly applicable across different cases. Electro-Acupuncture Treatment: Frequency: 3 sessions per week for 3 weeks. Needle retention time: ~30 minutes per session. Electroacupuncture at a frequency of 2 Hz Electroacupuncture Stimulation Parameters Electroacupuncture will be administered at a frequency of 2 Hz, as this has been shown to stimulate the release of endogenous opioids, including endorphins and enkephalins. These neuropeptides contribute to pain modulation and inflammation reduction via activation of the body's natural analgesic pathways (7). Additionally, low-frequency stimulation at 2 Hz has been associated with parasympathetic nervous system activation, which may further enhance pain relief by reducing stress-related sympathetic activity and promoting a relaxed physiological state. This dual mechanism makes 2 Hz electroacupuncture a suitable intervention for chronic and inflammatory pain conditions. Electrode placement and treatment duration will be standardized across participants to ensure consistency in stimulation intensity, needle depth, and session frequency. Acupuncture is dose-dependent, its effectiveness is influenced by treatment frequency and duration. It is thought more frequent sessions help reinforce therapeutic effects, particularly for chronic conditions. Treating pelvic pain from suspected endometriosis three times per week for three weeks ensures consistent stimulation of acupuncture points, for a sustained effect. Standardized point description KI-14 (Sì Mǎn) Location: 2 cun below the umbilicus and 0.5 cun lateral to the midline Needle Angle: Perpendicular insertion 0.5 to 1 cun Depth: Avoid deep needling to prevent penetrating peritoneal cavity in thin patients ST-28 (Shuidao) Location: 3 cun inferior to the umbilicus and 2 cun lateral to the midline, in the lower abdomen. Needle Angle: Perpendicular. Depth: 0.5-1.5 cun. Caution: Avoid deep needling to prevent injury to the peritoneal cavity in thin patients. LI 4 (Hegu) Location: On the dorsum of the hand, between the first and second metacarpal bones, at the midpoint of the second metacarpal bone, close to its radial border. Needle Angle: Perpendicular or oblique proximally toward the wrist. Depth: 0.5-1.0 cun. Contraindicated in pregnancy. Liv 3 (Tai Chong) Location: On the dorsum of the foot, in the depression distal to the junction of the first and second metatarsal bones. Needle Angle: Perpendicular or slightly oblique toward the first metatarsal space. Depth: 0.5-1.5 cun. Sp 6 (Sanyinjiao) Location: 3 cun superior to the prominence of the medial malleolus, on the posterior border of the tibia. Needle Angle: Perpendicular or oblique proximally. Depth: 0.5-1.5 cun. Contraindicated in pregnancy Sp 8 (Diji) Location: 3 cun inferior to Sp 9, on the line connecting Sp 9 and the medial malleolus, on the posterior border of the tibia. Needle Angle: Perpendicular. Depth: 0.5-1.5 cun. SP-10 (Xuehai) Location: On the medial aspect of the thigh, 2 cun superior to the superior border of the patella, in the bulge of the vastus medialis muscle. Needle Angle: Perpendicular. Depth: 0.5-1.5 cun. Traditional Considerations of Acupuncture Point Protocol SP6 (Sanyinjiao) - Regulates the uterus, calms pain SP8 (Diji) - for acute dysmenorrhea LV3 (Taichong) - Moves Liver Qi, reduces stagnation-related pain. Commonly used for menstrual pain, and stress relief. SP-10 (Xuehai) Regulates Menstruation,for menstrual disorders related to blood deficiency or stasis. Ki14 (Sì Mǎn) Moves Qi and Blood, alleviating pain, Irregular menstruation, dysmenorrhea ST-28 (Shuidao) - Regulates Menstruation \& the Uterus, Common in gynecological treatments. LI4 (Hegu) is known for its strong analgesic (pain-relieving) effects and is often used for headaches, facial pain, and general pain syndromes. Acupuncture Needles This study will use Scarborough CJ100 acupuncture needles (0.25mm gauge, 25mm length). These needles are made from surgical-grade stainless steel (SUS304) with a coiled copper handle and loop, traditional to Chinese acupuncture. They are silicone-coated for smooth insertion and come with a guide tube for precise placement. ES-130 Electroacupuncture Unit - Waveform and Current ES-130 electroacupuncture unit uses an asymmetric bi-phasic pulse waveform with a phase duration of 100µs. For this study, a 2Hz current will be applied, selected from the unit's adjustable frequency range of 0-500Hz. This specific frequency is chosen for its effect on endorphin release and pain modulation (5, 8).
- Outcome Measures Primary Outcomes: Changes in pain intensity measured via validated pain scale NRS (9, 10). Strongest, weakest, average pain last week + actual pain, all NRS scale 0 - 10 Pain catastrophizing scale (11) Type of pain (12) Amsterdam complex pelvic pain scale (13) Changes in quality of life (QoL) using a standardized questionnaire SF-36 (14). Change in pain medication use Secondary Outcomes: Changes in sexual function (FSFI, FSDS-r)(15) Pelvic ultrasound findings as an objective measure of muscle contractility (16) Changes in levator hiatal area at rest and contraction. Changes in levator hiatal anteroposterior diameter. Other outcomes from World endometriosis research foundation questionnaire User experience: How did the women experience participation in trial? What do they suggest could be done differently in future larger scale study?
- Data Collection \& Analysis Pre-treatment baseline assessment: Questionnaires Ultrasound Post-treatment assessment: At the end of the 3-week acupuncture period Questionnaires Follow-up assessments: At 2-3 months post-treatment (day of surgery) Questionnaires Ultrasound Result of surgery: confirmation of endometriosis at surgery according to revised American Fertility Society Score and histologically or other explanation to pain (adherances etc)
- Statistics Descriptive statistics for background variables Changes in outcomes over time: Mixed models Changes in outcomes at day of surgery between intervention and control group: t-test and Mann-Whitney U-test
- Power analyses We used this web page for power analyses: Power/Sample Size Calculator We assume that women have NRS 8 at inclusion and that women receiving acupuncture have a reduction to NRS 5 at day of surgery (SD 3). With a power and 0.8 and p-value 0.05, we would need 16 women in each group. We assume that we lose to follow up some participants, and will need to recruit 36 women, 18 in each group.
- Risks and benefits, Clinical relevance Acupuncture is a low risk treatment method, with minimal risk of adverse events (skin infection at insertion site, mild pain) It is time consuming to fill in the questionnaire and meet for treatment Potential benefit for each woman is pain relief
Clinical relevance Surgery is expensive and medication has side effects If EA turns out to be effective as pain relief for women with chronic pelvic pain, this may benefit future patents.
- Conditions
- Pelvic Pain, Endometriosis
- Being tested
- Electro acupuncture
- Keywords
- pelvic pain, endometriosis, acupuncture, sexual function, quality of life, pelvic floor muscle function
- Medical subject headings
- Pelvic Pain, Endometriosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Electro acupunctureDevice
Frequency: 3 sessions per week for 3 weeks. Needle retention time: ~30 minutes per session. Electroacupuncture at a frequency of 2 Hz Electroacupuncture Stimulation Parameters Electroacupuncture will be administered at a frequency of 2 Hz, as this has been shown to stimulate the release of endogenous opioids, including endorphins and enkephalins. These neuropeptides contribute to pain modulation and inflammation reduction via activation of the body's natural analgesic pathways (7). Additionally, low-frequency stimulation at 2 Hz has been associated with parasympathetic nervous system activation, which may further enhance pain relief by reducing stress-related sympathetic activity and promoting a relaxed physiological state. This dual mechanism makes 2 Hz electroacupuncture a suitable intervention for chronic and inflammatory pain conditions. Electrode placement and treatment duration will be standardized across participants to ensure consistency in stimulation intensity, needle depth
| Study group | Role | What they receive |
|---|---|---|
| Intervention, electroacupuncture | Experimental | Frequency: 3 sessions per week for 3 weeks. Needle retention time: ~30 minutes per session. Electroacupuncture at a frequency of 2 Hz Electroacupuncture Stimulation Parameters Electroacupuncture will be administered at a frequency of 2 Hz, as this has been shown to stimulate the release of endogenous opioids, including endorphins and enkephalins. These neuropeptides contribute to pain modulation and inflammation reduction via activation of the body's natural analgesic pathways (7). Additionally, low-frequency stimulation at 2 Hz has been associated with parasympathetic nervous system activation, which may further enhance pain relief by reducing stress-related sympathetic activity and promoting a relaxed physiological state. This dual mechanism makes 2 Hz electroacupuncture a suitable intervention for chronic and inflammatory pain conditions. Electrode placement and treatment duration will be standardized across participants to ensure consistency in stimulation intensity, needle depth Receives: Device: Electro acupuncture |
| Control | No intervention | Waiting as usual prior to surgery |
What is being measured
The primary outcome is the main question the study is designed to answer.
NRS
Changes in pain intensity measured via validated pain scale NRS
Measured: Baseline, after three months, and the day of surgery, average 6 months after baseline
Quality of life SF-36
standardized questionnaire measuring quality of life (SF-36)
Measured: Baseline, after three months, and the day of surgery, average 6 months after baseline
Change in pain medication use
Change in pain medication use
Measured: Baseline, after three months, and the day of surgery, average 6 months after baseline
Amsterdam complex pelvic pain scale
Changes in Amsterdam complex pelvic pain scale
Measured: Baseline, after three months, and the day of surgery, average 6 months after baseline
Secondary outcomes (3)
FSFI
Changes in sexual function FSFI
Measured: Baseline, after three months, and the day of surgery, average 6 months after baseline
FSDS-r
Changes in sexual function (FSDS-r)
Measured: Baseline, after three months, and the day of surgery, average 6 months after baseline
levator hiatal dimensions
Chenges in levator hiatal area and anteroposterior diameter measured at rest and contraction
Measured: Baseline and the day of surgery, average 6 months after baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Dec 2025
- Study start16 Dec 2025
- Primary completion31 Dec 2026 (estimated)
- Study completion30 Apr 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pelvic PainStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 38 participants (estimated)
Sponsor and investigators
- Lead sponsor
- St. Olavs Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Ingrid Volløyhaug, PhD, Principal investigator, St.Olavs Hopsital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07305025
- Sponsor's protocol ID
- REK 910176
- Acronym
- PEARL
- Status last verified
- Jul 2026
- First submitted
- 19 Nov 2025
- Last updated
- 21 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: few participants included. It might be possibel to identify study participants based on characteristica such as day of surgery, age, BMI
Study at a glance
From the registry record, last updated by the sponsor on 21 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pelvic Pain Electro-Acupuncture: Randomized Study for Symptom Liberation
- ClinicalTrials.gov ID
- NCT07305025
- Acronym / sponsor ID
- PEARL / REK 910176
- Conditions
- Pelvic Pain, Endometriosis
- Keywords
- pelvic pain, endometriosis, acupuncture, sexual function, quality of life, pelvic floor muscle function
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 38 participants (estimated)
- Lead sponsor
- St. Olavs HospitalUniversity, hospital or other
- Study start
- 16 Dec 2025 (actual)
- Primary completion
- 31 Dec 2026 (estimated)
- Study completion
- 30 Apr 2027 (estimated)
- First posted
- 26 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of the study is to investigate if a series of up to 9 treatment sessions of electroacupuncture can be used to alleviate pain in women with suspected endometriosis, scheduled for diagnostic laparoscopy
Detailed description
- Introduction Background: Endometriosis is a chronic inflammatory condition associated with significant pelvic pain, often requiring medical intervention. Globally, it is estimated that approximately 10 percent of reproductive-age females have endometriosis (1). Up to 70% of adolescent and adult females presenting for evaluation of chronic pelvic pain are diagnosed with endometriosis. While surgery and hormonal therapy are standard treatments, they may not be suitable or readily available for all patients. In addition, surgery is expensive and carries risk of complications. A systematic review and meta-analysis from 2023 including 331 women from six studies showed that acupuncture reduced overall pelvic pain and menstrual pain, but the evidence was low to moderate (2). The studies were non homogeneous regarding acupuncture style (Traditional Chinese, Japanese, ear acupuncture or unspecified), number of needles and duration of treatment. Another review from 2024 included 11 studies from China and three from other countries using different acupuncture techniques (3). They conclude that acupuncture is effective in alleviating dysmenorrhea and pelvic pain but the current evidence is limited and research focusing on subtypes of acupuncture is needed (3). Electro-acupuncture (EA) has been suggested as a promising approach to modulating pain perception and reducing inflammation. By influencing endogenous opioid release, regulating inflammatory cytokines, and improving pelvic blood flow, EA may provide effective symptom relief (4, 5). EA was more effective than conventional acupuncture in treating endometriosis related pain in a few studies (3, 6). Most previous studies are from China, and feasibility studies regarding type of acupuncture, duration of treatment, how women tolerate intervention and results on pelvic pain in a European setting are needed. Given the need for additional management options, particularly for women awaiting surgery or seeking alternatives to hormonal treatments, EA could offer valuable support in symptom relief. Aim: Primary aim: To assess the effect of acupuncture on pelvic pain in women with suspected endometriosis. Secondary aims: To assess the effect of acupuncture on pelvic floor muscle function, sexual function, quality of life. To determine feasibility for a larger-scale study.
- Study Design Type: Randomized Controlled Trial, Pilot study, non-blinded. Sample Size: 36 women with suspected endometriosis randomized to either acupuncture treatment or standard care. Women in the acupuncture group (n=18) will receive treatment in separate 3-week periods/blocks. Duration: Three weeks of acupuncture treatment with follow-up at end of treatment and 2-3 months post-treatment (day of surgery).
- Inclusion \& Exclusion Criteria Inclusion Criteria: Women aged 18-45 years referred for diagnostic laparoscopy with suspicion of endometriosis Experiencing moderate to severe pelvic pain Willing to commit to the treatment schedule and follow-up Understanding Norwegian or English to be able to communicate and fill out questionnaires Exclusion Criteria: Pregnancy Use of opioid pain relief Concurrent participation in other pain management trials.
- Intervention Rationale for point selection: Traditional Chinese Medicine (TCM) approaches treatment based on pattern differentiation, where diagnosis is guided by symptom presentation and observable signs. TCM recognizes multiple patterns for conditions like endometriosis, typically six distinct patterns. A key concept in TCM related to endometriosis is "qi and blood stagnation," a term that describes symptoms such as distension or sharp pain. While all cases of endometriosis in TCM include aspects of this pattern, the underlying TCM causes may vary. This protocol is designed to address the clinical presentation associated with qi and blood stagnation, making it standardized and broadly applicable across different cases. Electro-Acupuncture Treatment: Frequency: 3 sessions per week for 3 weeks. Needle retention time: ~30 minutes per session. Electroacupuncture at a frequency of 2 Hz Electroacupuncture Stimulation Parameters Electroacupuncture will be administered at a frequency of 2 Hz, as this has been shown to stimulate the release of endogenous opioids, including endorphins and enkephalins. These neuropeptides contribute to pain modulation and inflammation reduction via activation of the body's natural analgesic pathways (7). Additionally, low-frequency stimulation at 2 Hz has been associated with parasympathetic nervous system activation, which may further enhance pain relief by reducing stress-related sympathetic activity and promoting a relaxed physiological state. This dual mechanism makes 2 Hz electroacupuncture a suitable intervention for chronic and inflammatory pain conditions. Electrode placement and treatment duration will be standardized across participants to ensure consistency in stimulation intensity, needle depth, and session frequency. Acupuncture is dose-dependent, its effectiveness is influenced by treatment frequency and duration. It is thought more frequent sessions help reinforce therapeutic effects, particularly for chronic conditions. Treating pelvic pain from suspected endometriosis three times per week for three weeks ensures consistent stimulation of acupuncture points, for a sustained effect. Standardized point description KI-14 (Sì Mǎn) Location: 2 cun below the umbilicus and 0.5 cun lateral to the midline Needle Angle: Perpendicular insertion 0.5 to 1 cun Depth: Avoid deep needling to prevent penetrating peritoneal cavity in thin patients ST-28 (Shuidao) Location: 3 cun inferior to the umbilicus and 2 cun lateral to the midline, in the lower abdomen. Needle Angle: Perpendicular. Depth: 0.5-1.5 cun. Caution: Avoid deep needling to prevent injury to the peritoneal cavity in thin patients. LI 4 (Hegu) Location: On the dorsum of the hand, between the first and second metacarpal bones, at the midpoint of the second metacarpal bone, close to its radial border. Needle Angle: Perpendicular or oblique proximally toward the wrist. Depth: 0.5-1.0 cun. Contraindicated in pregnancy. Liv 3 (Tai Chong) Location: On the dorsum of the foot, in the depression distal to the junction of the first and second metatarsal bones. Needle Angle: Perpendicular or slightly oblique toward the first metatarsal space. Depth: 0.5-1.5 cun. Sp 6 (Sanyinjiao) Location: 3 cun superior to the prominence of the medial malleolus, on the posterior border of the tibia. Needle Angle: Perpendicular or oblique proximally. Depth: 0.5-1.5 cun. Contraindicated in pregnancy Sp 8 (Diji) Location: 3 cun inferior to Sp 9, on the line connecting Sp 9 and the medial malleolus, on the posterior border of the tibia. Needle Angle: Perpendicular. Depth: 0.5-1.5 cun. SP-10 (Xuehai) Location: On the medial aspect of the thigh, 2 cun superior to the superior border of the patella, in the bulge of the vastus medialis muscle. Needle Angle: Perpendicular. Depth: 0.5-1.5 cun. Traditional Considerations of Acupuncture Point Protocol SP6 (Sanyinjiao) - Regulates the uterus, calms pain SP8 (Diji) - for acute dysmenorrhea LV3 (Taichong) - Moves Liver Qi, reduces stagnation-related pain. Commonly used for menstrual pain, and stress relief. SP-10 (Xuehai) Regulates Menstruation,for menstrual disorders related to blood deficiency or stasis. Ki14 (Sì Mǎn) Moves Qi and Blood, alleviating pain, Irregular menstruation, dysmenorrhea ST-28 (Shuidao) - Regulates Menstruation \& the Uterus, Common in gynecological treatments. LI4 (Hegu) is known for its strong analgesic (pain-relieving) effects and is often used for headaches, facial pain, and general pain syndromes. Acupuncture Needles This study will use Scarborough CJ100 acupuncture needles (0.25mm gauge, 25mm length). These needles are made from surgical-grade stainless steel (SUS304) with a coiled copper handle and loop, traditional to Chinese acupuncture. They are silicone-coated for smooth insertion and come with a guide tube for precise placement. ES-130 Electroacupuncture Unit - Waveform and Current ES-130 electroacupuncture unit uses an asymmetric bi-phasic pulse waveform with a phase duration of 100µs. For this study, a 2Hz current will be applied, selected from the unit's adjustable frequency range of 0-500Hz. This specific frequency is chosen for its effect on endorphin release and pain modulation (5, 8).
- Outcome Measures Primary Outcomes: Changes in pain intensity measured via validated pain scale NRS (9, 10). Strongest, weakest, average pain last week + actual pain, all NRS scale 0 - 10 Pain catastrophizing scale (11) Type of pain (12) Amsterdam complex pelvic pain scale (13) Changes in quality of life (QoL) using a standardized questionnaire SF-36 (14). Change in pain medication use Secondary Outcomes: Changes in sexual function (FSFI, FSDS-r)(15) Pelvic ultrasound findings as an objective measure of muscle contractility (16) Changes in levator hiatal area at rest and contraction. Changes in levator hiatal anteroposterior diameter. Other outcomes from World endometriosis research foundation questionnaire User experience: How did the women experience participation in trial? What do they suggest could be done differently in future larger scale study?
- Data Collection \& Analysis Pre-treatment baseline assessment: Questionnaires Ultrasound Post-treatment assessment: At the end of the 3-week acupuncture period Questionnaires Follow-up assessments: At 2-3 months post-treatment (day of surgery) Questionnaires Ultrasound Result of surgery: confirmation of endometriosis at surgery according to revised American Fertility Society Score and histologically or other explanation to pain (adherances etc)
- Statistics Descriptive statistics for background variables Changes in outcomes over time: Mixed models Changes in outcomes at day of surgery between intervention and control group: t-test and Mann-Whitney U-test
- Power analyses We used this web page for power analyses: Power/Sample Size Calculator We assume that women have NRS 8 at inclusion and that women receiving acupuncture have a reduction to NRS 5 at day of surgery (SD 3). With a power and 0.8 and p-value 0.05, we would need 16 women in each group. We assume that we lose to follow up some participants, and will need to recruit 36 women, 18 in each group.
- Risks and benefits, Clinical relevance Acupuncture is a low risk treatment method, with minimal risk of adverse events (skin infection at insertion site, mild pain) It is time consuming to fill in the questionnaire and meet for treatment Potential benefit for each woman is pain relief
Clinical relevance Surgery is expensive and medication has side effects If EA turns out to be effective as pain relief for women with chronic pelvic pain, this may benefit future patents.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention, electroacupuncture | Experimental | Device: Electro acupunctureFrequency: 3 sessions per week for 3 weeks. Needle retention time: ~30 minutes per session. Electroacupuncture at a frequency of 2 Hz Electroacupuncture Stimulation Parameters Electroacupuncture will be administered at a frequency of 2 Hz, as this has been shown to stimulate the release of endogenous opioids, including endorphins and enkephalins. These neuropeptides contribute to pain modulation and inflammation reduction via activation of the body's natural analgesic pathways (7). Additionally, low-frequency stimulation at 2 Hz has been associated with parasympathetic nervous system activation, which may further enhance pain relief by reducing stress-related sympathetic activity and promoting a relaxed physiological state. This dual mechanism makes 2 Hz electroacupuncture a suitable intervention for chronic and inflammatory pain conditions. Electrode placement and treatment duration will be standardized across participants to ensure consistency in stimulation intensity, needle depth |
| Control | No intervention | –Waiting as usual prior to surgery |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- Women aged 18-45 years referred for diagnostic laparoscopy with suspicion of endometriosis
- Experiencing moderate to severe pelvic pain
- Willing to commit to the treatment schedule and follow-up
- Understanding Norwegian or English to be able to communicate and fill out questionnaires
Key exclusion criteria (3 listed)
- Pregnancy
- Use of opioid pain relief
- Concurrent participation in other pain management trials
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Electro acupunctureFrequency: 3 sessions per week for 3 weeks. Needle retention time: ~30 minutes per session. Electroacupuncture at a frequency of 2 Hz Electroacupuncture Stimulation Parameters Electroacupuncture will be administered at a frequency of 2 Hz, as this has been shown to stimulate the release of endogenous opioids, including endorphins and enkephalins. These neuropeptides contribute to pain modulation and inflammation reduction via activation of the body's natural analgesic pathways (7). Additionally, low-frequency stimulation at 2 Hz has been associated with parasympathetic nervous system activation, which may further enhance pain relief by reducing stress-related sympathetic activity and promoting a relaxed physiological state. This dual mechanism makes 2 Hz electroacupuncture a suitable intervention for chronic and inflammatory pain conditions. Electrode placement and treatment duration will be standardized across participants to ensure consistency in stimulation intensity, needle depth | Device | Intervention, electroacupuncture |
Primary outcome
NRS
Time frame: Baseline, after three months, and the day of surgery, average 6 months after baseline
Changes in pain intensity measured via validated pain scale NRS
Quality of life SF-36
Time frame: Baseline, after three months, and the day of surgery, average 6 months after baseline
standardized questionnaire measuring quality of life (SF-36)
Change in pain medication use
Time frame: Baseline, after three months, and the day of surgery, average 6 months after baseline
Change in pain medication use
Amsterdam complex pelvic pain scale
Time frame: Baseline, after three months, and the day of surgery, average 6 months after baseline
Changes in Amsterdam complex pelvic pain scale
3 secondary outcomes
FSFI
Time frame: Baseline, after three months, and the day of surgery, average 6 months after baseline
FSDS-r
Time frame: Baseline, after three months, and the day of surgery, average 6 months after baseline
levator hiatal dimensions
Time frame: Baseline and the day of surgery, average 6 months after baseline
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Jul 2026.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: No. few participants included. It might be possibel to identify study participants based on characteristica such as day of surgery, age, BMI
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Ingrid Volløyhaug, PhD principal investigator
St.Olavs Hopsital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Electro acupuncture in people with Pelvic Pain and Endometriosis, run by St. Olavs Hospital at 1 site in Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. 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: looking for participants now, as of the sponsor's last update on 21 Jul 2026. 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 Norway. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Ingrid Volløyhaug, PhD (+47 72573831, ingrid.volloyhaug@ntnu.no), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
NRS (time frame: Baseline, after three months, and the day of surgery, average 6 months after baseline). The study lists 4 primary outcomes in all. 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 21 Jul 2026.