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HemorrhoidsPINPOINTNCT07813338

Pudendal Nerve Block Techniques for Pain Control After Hemorrhoidectomy

A study testing Transgluteal Pudendal Nerve Block and Transperineal pudendal nerve block in people with Hemorrhoids and Postoperative Pain, run by Vinmec Healthcare System.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Hemorrhoidectomy is frequently associated with severe postoperative pain despite multimodal analgesia. Ultrasound-guided pudendal nerve block has become an effective regional analgesic technique, but it remains unknown whether blockade performed proximally at the ischial spine provides superior analgesia compared with… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Hemorrhoids, Postoperative Pain
What is being tested?
Transgluteal Pudendal Nerve Block and Transperineal pudendal nerve block
Could I receive a placebo?
No, everyone receives an active treatment
How many people
140 participants
Where
No sites listed yet
Study dates
15 Sep 2026to 30 Sep 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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adults aged 18 years or older.
  • Scheduled for elective hemorrhoidectomy.
  • Hemorrhoidectomy performed using either the Milligan-Morgan or Ferguson technique.
  • ASA Physical Status I-III.
  • Able to understand the study procedures and provide written informed consent.
  • Able to complete postoperative pain and quality-of-recovery assessments.

Who cannot join

  • Chronic opioid use exceeding 30 mg morphine milligram equivalents per day.
  • Known allergy or contraindication to local anesthetics.
  • Coagulopathy or other contraindication to peripheral nerve block.
  • Infection at the planned injection site.
  • Pregnancy.
  • Cognitive impairment preventing reliable completion of study questionnaires or pain assessments.

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Philippe B Macaire, MD contact

+84 0966103845

ph.macaire@gmail.com

Nguyen H Thoai, MD contact

+84 0974944472

v.thoainh3@vinmec.com

About this study

Official title: Transgluteal Versus Transperineal Pudendal Nerve Block for Analgesia After Hemorrhoidectomy: A Randomized Superiority Trial (The PINPOINT Trial)

Hemorrhoidectomy is frequently associated with severe postoperative pain despite multimodal analgesia. Ultrasound-guided pudendal nerve block has become an effective regional analgesic technique, but it remains unknown whether blockade performed proximally at the ischial spine provides superior analgesia compared with the more distal transperineal approach.

The PINPOINT Trial is a prospective randomized assessor-blinded superiority trial comparing ultrasound-guided transgluteal (proximal) and transperineal (distal) pudendal nerve block in adults undergoing elective hemorrhoidectomy. The primary objective is to determine whether the proximal approach reduces cumulative opioid consumption during the first 48 postoperative hours. Secondary outcomes include pain intensity, opioid-related outcomes, recovery, complications, and patient-reported outcomes.

Read the detailed description

Context, rationale and hypothesis: Hemorrhoidectomy remains one of the most painful ambulatory surgical procedures, frequently associated with substantial postoperative opioid consumption despite multimodal analgesia. This persistent nociceptive burden has direct implications for delayed recovery, unplanned admissions, and opioid-related adverse events. Consequently, optimizing regional analgesic strategies is a priority within enhanced recovery pathways.

Pudendal nerve block (PNB), targeting sacral roots S2-S4, has emerged as an effective adjunct for postoperative analgesia in anorectal surgery. Randomized trials and meta-analyses consistently demonstrate reductions in pain scores and opioid requirements when PNB is incorporated into perioperative care. However, these studies encompass heterogeneous techniques, and critically, do not address whether the anatomical level of blockade influences clinical efficacy.

From a mechanistic perspective, the pudendal nerve divides into its terminal branches-the inferior rectal, perineal, and dorsal genital nerves-after traversing the region of the ischial spine and entering Alcock's canal. The inferior rectal nerve, which provides the principal sensory innervation to the anal canal and perianal region, typically branches proximally before the pudendal nerve courses distally within the pudendal canal. This anatomical arrangement suggests that distal approaches to PNB, such as the transperineal technique, may incompletely anesthetize the inferior rectal nerve due to injection beyond the point of branching or variable spread within the ischiorectal fossa.

In contrast, the posterior transgluteal approach targets the pudendal nerve at a more proximal location, near the ischial spine and sacrospinous ligament, where the nerve remains a single trunk. Ultrasound guidance at this level enables precise deposition of local anesthetic before division into terminal branches, theoretically ensuring a more consistent and comprehensive blockade, including the inferior rectal nerve. This distinction in injection level-proximal versus distal-represents a fundamental but underexplored determinant of block success.

Despite increasing adoption of ultrasound-guided regional anesthesia, there is a striking absence of randomized controlled trials directly comparing proximal (transgluteal) and distal (transperineal) approaches to PNB in the context of hemorrhoidectomy. Existing evidence is therefore insufficient to determine whether improved anatomical coverage translates into superior clinical analgesia or reduced opioid consumption.

Addressing this gap is clinically relevant for several reasons. First, inadequate blockade of the inferior rectal nerve may contribute to residual pain during defecation, a key determinant of patient dissatisfaction after hemorrhoidectomy. Second, identifying a more reliable and reproducible technique could standardize PNB within perioperative protocols. Third, demonstrating superiority of a proximal approach would support broader integration of ultrasound-guided regional techniques into opioid-sparing strategies.

The present trial is designed to test the hypothesis that a proximal, ultrasound-guided transgluteal PNB provides superior postoperative analgesia compared with a distal transperineal approach. By directly comparing these techniques in a randomized controlled setting, this study seeks to determine whether anatomical optimization of nerve blockade translates into meaningful clinical benefit.

Originality and innovative aspects: Hemorrhoidectomy remains associated with significant postoperative pain, often requiring substantial opioid consumption. Pudendal nerve block (PNB), targeting nerve roots from S2-S4, has demonstrated efficacy in reducing postoperative pain and opioid requirements. Anatomically, the pudendal nerve gives rise to the inferior rectal, perineal, and dorsal genital nerves. The effectiveness of PNB depends on the level of injection:

  • Transgluteal (proximal) approach: blockade at the level of the ischial spine before nerve branching
  • Transperineal (distal) approach: injection within or near Alcock's canal after branching The distal approach may spare the inferior rectal nerve, leading to suboptimal anorectal analgesia. In contrast, the proximal ultrasound-guided technique may provide a more complete and reliable block.

To date, no randomized controlled trial has directly compared proximal (transgluteal) and distal (transperineal) approaches to pudendal nerve block in hemorrhoidectomy, despite clear anatomical rationale suggesting differences in nerve coverage and analgesic efficacy.

Methods This study is a prospective, Randomized, Controlled, Parallel-group , Superiority trial, Assessor-blinded The protocol follows SPIRIT recommendations, and reporting will adhere to CONSORT guidelines Setting The study will be conducted at VinMec International Hospital, Can THo, Vietnam. Interventions Control Group (Standard Management): Trans perineal Group (Distal PNB) Spinal anesthesia protocol standardized; Ultrasound-guided transperineal approach ; Injection in rectoperineal/ischiorectal fossa; Bilateral; Ropivacaine 0. 5%, 8 mL per side; Oral Paracetamol 500 mg every 6 hours; Oral Celecoxib 200 mg every 12 hours ( if no contra-indication); Rescue opioids if NRS pain values >3/10 converted to MME Intervention Group: Transgluteal Group (Proximal PNB) General anesthesia protocol standardized; Ultrasound-guided posterior approach; Injection near ischial spine/sacrospinous ligament; Bilateral; Ropivacaine 0. 5%, 6 mL per side; Oral Paracetamol 500 mg every 6 hours; Oral Celecoxib 200 mg every 12 hours (if no contra-indication); Rescue opioids if NRS pain values >3/10 converted to MME

The Block Techniques:

Transperineal Approach Patient Positioning The patient is placed in the lithotomy position with slight hip abduction. Adequate exposure of the perineum is ensured under strict aseptic conditions.

Ultrasound Equipment and Probe Position A high-frequency linear transducer (10-18 MHz) is used. The probe is placed: Transversely or slightly oblique; On the perineum, lateral to the external anal sphincter; Over the ischio-rectal fossa.

Sonoanatomy Key structures to identify include: External anal sphincter (medial landmark); Ischioanal (ischiorectal) fossa (hypoechoic fat-filled space); Obturator internus muscle (lateral boundary); Internal pudendal artery (identified using color Doppler). The pudendal nerve is often not directly visualized, but lies medial to the internal pudendal artery and within or near Alcock's (pudendal) canal Needle Insertion Approach: in-plane, typically medial to lateral; Needle: 50mm echogenic needle advanced to the ischioanal fossa, adjacent to the internal pudendal artery.

Injection 8 mL of local anesthetic is injected per side. The spread should be observed within the ischioanal fossa Controlled by Color echo Doppler to prevent IV injection.

Transgluteal Approach Patient Positioning The patient is placed in the prone position (or lateral decubitus if needed). The gluteal region is exposed and prepared under sterile conditions.

Ultrasound Equipment and Probe Position A low-frequency curvilinear probe (2-5 MHz) or a high-frequency probe in lean patients may be used.

The probe is positioned transversely over the gluteal region, at the level of the ischial spine Sonoanatomy Key landmarks: Ischial spine (hyperechoic bony structure with acoustic shadow); Sacrospinous ligament; Sacrotuberous ligament; Internal pudendal artery (identified with Doppler). The pudendal nerve is located medial and posterior to the internal pudendal artery between the sacrospinous and sacrotuberous ligaments. It may appear as a small hyperechoic oval structure, although visualization is variable.

Needle Insertion Approach: in-plane, usually lateral-to-medial; Needle: 50 or 80 mm echogenic needle. The needle is advanced through the gluteal muscles, toward the ischial spine region, Into the interligamentous plane (between sacrospinous and sacrotuberous ligaments) Injection 6 mL of local anesthetic is injected per side. The spread of LA expands of the interligamentous space, circumferential spread around the pudendal artery controlled by Color echo doppler Sample Size: Assuming a mean 48h opioid consumption at 60 mg MME with a standard deviation: 30 mg and a clinically meaningful difference of 15 mg (25% reduction) with an Alpha risk : 0.05 (two-sided) and a β risk Power: 80%, the required sample is 64 patients per group. Accounting for 10% dropout the Total sample size: 140 patients (70 per group).

Analysis of the Population: Intention-to-treat (ITT) (primary analysis) and Per-protocol (sensitivity analysis) Descriptive Statistics: Continuous variables: mean ± SD or median (IQR) and Categorical variables: n (%)

Primary Outcome Analysis:

Comparison of cumulative MME at 48 h: If normally distributed → Student's t-test; If non-normal → Mann-Whitney U test Additionally: Linear regression adjusted for: Age, Sex, Surgical technique, Baseline pain Effect size: Mean difference with 95% confidence interval

Secondary Analyses :

Pain scores (repeated measures): Mixed-effects linear models ; Fixed effects: group, time, group × time interaction; Random intercept for patient

Time-to-event outcomes:

Time to first opioid: Kaplan-Meier analysis; Log-rank test; Cox proportional hazards model

Categorical outcomes:

Chi-square or Fisher's exact test; Report relative risks with 95% CI

Continuous outcomes:

t-test or Mann-Whitney depending on distribution Handling Missing Data : Multiple imputation if >5% missing; Sensitivity analyses Significance Threshold : p < 0.05 (two-sided) Randomization Randomization and Blinding : Allocation ratio: 1:1; Computer-generated random sequence with variable block sizes; Allocation concealment via secure electronic system

Blinding:

The patients are blinded; Outcome assessors: blinded; Data analysts: blinded; Performing anesthesiologist: not blinded Data Collection Methods: Pain opiates consumption and functional outcomes will be assessed at predefined time points using scales and validated questionnaires: NRS pain score at rest and during movement, .Lickert scale for patient satisfaction, consumption of rescue analgesia opiates (MME), Brief Pain Inventory and QOR 15 form. Data will be collected during follow-up visits or via structured interviews.

Being tested
Transgluteal Pudendal Nerve Block, Transperineal pudendal nerve block
Keywords
Hemorrhoidectomy, Pudendal Nerve Block, Regional Anesthesia, Ultrasound-Guided Nerve Block, Postoperative Pain, Opioid Consumption, Enhanced Recovery
Medical subject headings
Hemorrhoids, Pain, Postoperative

What participants receive

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

  • Transgluteal Pudendal Nerve BlockProcedure or surgery

    Participants will receive bilateral ultrasound-guided posterior transgluteal pudendal nerve blocks under standardized general anesthesia. With the patient prone or in lateral decubitus, the gluteal region will be prepared aseptically. Ultrasound and color Doppler will identify the ischial spine, sacrospinous and sacrotuberous ligaments, and internal pudendal artery. An in-plane needle will be advanced into the interligamentous target plane, followed by injection of 5 mL ropivacaine 0.5% on each side. Local anesthetic spread will be assessed sonographically. Postoperative analgesia will include paracetamol and celecoxib when appropriate, with rescue opioids given for NRS pain >3/10. Opioid consumption will be converted to morphine milligram equivalents (MME) for analysis.

  • Transperineal pudendal nerve blockProcedure or surgery

    Participants will receive bilateral ultrasound-guided transperineal pudendal nerve blocks following standardized general anesthesia. In lithotomy position, the perineum will be prepared aseptically. A high-frequency ultrasound probe will identify the relevant anatomical structures and the internal pudendal artery using Color Doppler. An echogenic needle will be advanced under ultrasound guidance into the ischioanal/ischiorectal fossa adjacent to the internal pudendal artery. After aspiration, 8 mL of 0.5% ropivacaine will be injected on each side, with ultrasound assessment of anesthetic spread. Postoperative analgesia will consist of standardized paracetamol and celecoxib. Rescue opioids will be administered for pain >3/10 and converted to morphine milligram equivalents (MME) for analysis.

Study groups in NCT07813338
Study groupRoleWhat they receive
Transgluteal pudendal nerve blockExperimentalUltrasound-guided bilateral transgluteal pudendal nerve block performed at the level of the ischial spine before pudendal nerve division.
Receives: Procedure: Transgluteal Pudendal Nerve Block
Transperineal Pudendal Nerve BlockActive comparatorUltrasound-guided bilateral transperineal pudendal nerve block performed within the ischiorectal fossa near Alcock's canal.
Receives: Procedure: Transperineal pudendal nerve block

What is being measured

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

  1. Cumulative post operative opioid consumption at 48 Hours (MME)

    Cumulative opioid consumption from the end of surgery through 48 hours after surgery, expressed as morphine milligram equivalents (MME). All postoperative opioid analgesics administered during the observation period will be converted to MME using the prespecified opioid conversion table.

    Measured: Post operative From the end of surgery to 48 hours after surgery

Secondary outcomes (10)
  1. post operative pain intensity at rest

    Pain intensity at rest measured by Visual Analogic Scale (VAS) ruller.

    Measured: post operative at 2 hours, 6 hours, 12 hours, 24 hours and 48 hours after end of surgery

  2. Post operative pain intensity during defecation

    Pain Intensity during defecation using Visual Analogic Scale (VAS) ruler

    Measured: at the first post operative defecation and during the first 48 hours post operative observation period.

  3. Pain Intensity-time area under the curve over 48 hours after the end of surgery

    Area under the curve of post operative VAS pain scores from end of the surgery through 48 hours.

    Measured: from end of the surgery to 48 hours after surgery

  4. cumulative post operative opioid consumption at 12 hours, 24 hours and 36 Hours

    cumulative post operative opioid consumption at 12 hours, 24 hours and 36 Hours expressed as morphine miligram equivalents (MME)

    Measured: Post operative : at 12 hours, 24 hours and 36 Hours after the surgery

  5. Time to first rescue opioid administration

    Time from end of surgery to the first rescue opioid administration

    Measured: Post operative : from end of surgery through 48 hours after surgery

  6. Proportion of participants who remain opioid free at 48 hours

    Proportion of participants who remain opioid free at 48 hours

    Measured: post operative : From end of surgery through 48 hours after surgery

  7. Quatilty of recovery assessed using the score QoR-15

    Post operative Quatilty of recovery assessed using the score QoR-15

    Measured: Post operative : 24 hours and 48 hours after the end of surgery

  8. Adverse events (Nausea Vomiting Urinary retention)

    Adverse events (Nausea Vomiting Urinary retention) from end of surgery through 48 hours after surgery

    Measured: Post operative : from end of surgery through 48 hours after surgery

  9. Block related complications

    Occurence of complications related to pudendal nerve block

    Measured: From block performance through 48 hours after surgery

  10. Length of hospital stay after surgery performed

    Length of hospital stay from end of surgery to hospital discharge

    Measured: duration of post operative hospitalization : From end of surgery to hospital discharge up to one week

Timeline

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

  1. First posted10 Sep 2026
  2. Study start15 Sep 2026 (estimated)
  3. Primary completion31 Aug 2027 (estimated)
  4. Study completion30 Sep 2027 (estimated)

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
Prospective, randomised, controlled, parallel groups, superiority trial with a 1:1 allocation ratio
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
140 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07813338
Sponsor's protocol ID
PINPOINT-01
Acronym
PINPOINT
Status last verified
Sep 2026
First submitted
17 Aug 2026
Last updated
10 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Publications

  • Levin D, Van Florcke D, Schmitt M, Kendall LK, Patel A, Doan LV, Kirpekar M. Fluoroscopy-Guided Transgluteal Pudendal Nerve Block for Pudendal Neuralgia: A Retrospective Case Series. J Clin Med. 2024 Apr 30;13(9):2636. doi: 10.3390/jcm13092636.

    PubMed 38731163
  • Kovacs P, Gruber H, Piegger J, Bodner G. New, simple, ultrasound-guided infiltration of the pudendal nerve: ultrasonographic technique. Dis Colon Rectum. 2001 Sep;44(9):1381-5. doi: 10.1007/BF02234802.

    PubMed 11584221
  • Soucy B, Luong DH, Michaud J, Boudier-Reveret M, Sobczak S. Accuracy of Ultrasound-Guided Pudendal Nerve Block in the Ischial Spine and Alcock's Canal Levels: A Cadaveric Study. Pain Med. 2020 Nov 1;21(11):2692-2698. doi: 10.1093/pm/pnaa136.

    PubMed 32451530
  • Xia S, Luo L, Wu W, Lu K, Jiang T, Li Y. The role of pudendal nerve block in hemorrhoid surgery: a systematic review and meta-analysis of double-blind randomized controlled trials. Front Med (Lausanne). 2023 Dec 13;10:1283512. doi: 10.3389/fmed.2023.1283512. eCollection 2023.

    PubMed 38152300
  • He J, Zhang L, Li DL, He WY, Xiong QM, Zheng XQ, Liao MJ, Wang HB. Ultrasound-Guided Pudendal Nerve Block Combined with Propofol Deep Sedation versus Spinal Anesthesia for Hemorrhoidectomy: A Prospective Randomized Study. Pain Res Manag. 2021 Feb 26;2021:6644262. doi: 10.1155/2021/6644262. eCollection 2021.

    PubMed 33727997
  • Mongelli F, Lucchelli M, La Regina D, Christoforidis D, Saporito A, Vannelli A, Di Giuseppe M. Ultrasound-Guided Pudendal Nerve Block in Patients Undergoing Open Hemorrhoidectomy: A Post-Hoc Cost-Effectiveness Analysis from a Double-Blind Randomized Controlled Trial. Clinicoecon Outcomes Res. 2021 Apr 28;13:299-306. doi: 10.2147/CEOR.S306138. eCollection 2021.

    PubMed 33953578
  • Bikfalvi A, Faes C, Freys SM, Joshi GP, Van de Velde M, Albrecht E. PROSPECT guideline for haemorrhoid surgery: A systematic review and procedure-specific postoperative pain management recommendations. Eur J Anaesthesiol Intensive Care. 2023 May 26;2(3):e0023. doi: 10.1097/EA9.0000000000000023. eCollection 2023 Jun.

    PubMed 39917290
  • Nadri S, Mahmoudvand H, Rokrok S, Tarrahi MJ. Comparison of Two Methods: Spinal Anesthesia and Ischiorectal Block on Post Hemorrhoidectomy Pain and Hospital Stay: A Randomized Control Trial. J Invest Surg. 2018 Oct;31(5):420-424. doi: 10.1080/08941939.2017.1349221. Epub 2017 Nov 27.

    PubMed 29172862
  • Naja Z, Ziade MF, Lonnqvist PA. Nerve stimulator guided pudendal nerve block decreases posthemorrhoidectomy pain. Can J Anaesth. 2005 Jan;52(1):62-8. doi: 10.1007/BF03018582.

    PubMed 15625258
  • Mongelli F, Treglia G, La Regina D, Di Giuseppe M, Galafassi J, Majno-Hurst PE, Christoforidis D. Pudendal Nerve Block in Hemorrhoid Surgery: A Systematic Review and Meta-analysis. Dis Colon Rectum. 2021 May;64(5):617-631. doi: 10.1097/DCR.0000000000001985.

    PubMed 33591044
  • Steen CJ, Lam D, Chandra R, Chua JYJ, An V, Keck JO. Pudendal Nerve Block for Posthemorrhoidectomy Pain: A Prospective, Single-Blinded Randomized Control Trial. Dis Colon Rectum. 2022 Apr 1;65(4):546-551. doi: 10.1097/DCR.0000000000002293.

    PubMed 34759239

Questions about this trial

What is this clinical trial studying?

A study testing Transgluteal Pudendal Nerve Block and Transperineal pudendal nerve block in people with Hemorrhoids and Postoperative Pain, run by Vinmec Healthcare System.

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 6 inclusion and 6 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: opening soon, as of the sponsor's last update on 10 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

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 Philippe B Macaire, MD (+84 0966103845, ph.macaire@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cumulative post operative opioid consumption at 48 Hours (MME) (time frame: Post operative From the end of surgery to 48 hours after surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07813338, which also lists 11 linked publications.

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 10 Sep 2026; AzTrials last refreshed its copy on 1 Nov 2026.

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