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CompletedNCT03181243Updated Jan 2, 2018

The Acceptance, Safety, and Efficacy of MadaJet Versus Needle Injection for Sperm Retrieval in Patients With Azoospermia

An interventional study of Madajet and Needle injection in Male Infertility, sponsored by Vietnam National University. Completed at 1 site in Vietnam. Open to male participants aged 20 Years to 100 Years. Per ClinicalTrials.gov, last updated 2018-01-02.

Sponsored by Vietnam National University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
20 Years to 100 Years
Sex
Male
01

Study summary

To compare the acceptance, safety, and efficacy of needle-free jet anaesthetic technique (MadaJet) versus needle injection for sperm retrieval in patients with azoospermia.

Read the detailed description

Azoospermia is found in 1-3% of general population and 10-15% of men presenting with infertility. In this scenario, there are no spermatozoa in the patient's semen after centrifugation, and pregnancy may be achieved through IVF/ Intracytoplasmic sperm injection (ICSI) combined with sperm retrieval techniques (e.g. PESA, testicular sperm extraction - TESE, TESA). These techniques are commonly conducted under local anesthesia, which a 10-15 mL solution of 2% lidocaine hydrochloride injected around the spermatic cord near the external inguinal ring. However, needle fear is prevalent in both children (\~33-63%) and adults (\~14-38%) and can contribute to negative experiences with needle procedures and health care for patients, caregivers, and health professionals. In clinical practice, patients often concern about the pain, trauma and possible complication (i.e. wheal, hematoma, infection) of needle injection of local anaesthesia into and through the scrotal wall when performing sperm retrieval. It not only interferes with clinicians' abilities to carry out procedures (e.g. due to flailing and attempts to escape), but also undermines the efficacy of pain interventions at the time of the needle. Therefore, receiving local anaesthesia without a needle is easily well accepted by the patients with azoospermia.

The needleless jet injector (MadaJet Medical Injector) has been widely used in the fields of dermatology, cosmetic and plastic surgery, gynecology, dentistry, and podiatry as well as for immunization. It was also employed for no-scalpel vasectomy in Urology/Andrology. The first studies using needleless jet injector for spermatic cord block was reported by Wilson in 2001 and Weiss in 2005. The next studies showed that MadaJet has better outcomes (e.g. cost, pain scores, onset time) than traditional needle anaesthesia (16-18). Unlike a conventional spermatic cord block with needle injection, there is no wheal on the patients' skin and local edema after administering injection. A mist of solution with a high-pressure injector will be rapidly delivered and absorbed through the skin to the tissue beneath around the cord with much less trauma. As a consequence, it is less painful than the needle injection.

For those reasons, a needle-free jet anaesthetic technique for sperm retrieval will be described for local anaesthesia, which may minimize the fear of the needle. The acceptance, safety, and efficacy of this technique will also be compared with needle injection for sperm retrieval in azoospermia patients.

02

Conditions studied

03

Who can participate

Ages eligible
20 Years to 100 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • Patients (including obstructive azoospermia and non-obstructive azoospermia) in need of sperm retrieval (PESA, TESE) for ICSI.

Exclusion criteria

Exclusion Criteria:

  • Have not finished the process of sperm retrieval techniques.
  • Malformation of genital organs (e.g. spermatic cord, testicle)
  • Anxious, alcoholic patients.
  • Patients giving a history of personality disorders.
  • Patients who abuse drugs.
  • Disagree to participate in the study.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    MadaJet

    Jet injector (Madajet medical Urology) preloaded as manufacturer's instruction

    Procedure: Madajet

  • Experimental
    Needle injection

    01 sterile 10-mL syringe with small gauge needle (25 ga), solution for sterile preparation, 10 - 15 mL Lidocaine 2%

    Procedure: Needle injection

Interventions

  • ProcedureMadajet

    The spermatic cord is firmly trapped between the middle finger, index finger and thumb of the left hand. The injector's sheath is placed over the spermatic cord with gentle pressure adjacent to the external inguinal ring. Depending upon the thickness of spermatic cord, three or four injections are consecutively administered around it, beginning from proximal to distal points.

    Also known as: Needle-free jet anaesthetic technique

  • ProcedureNeedle injection

    The pubic tubercle is palpated on the side that is going to be blocked. The spermatic cord is then immobilised with the non-dominant hand between the thumb and index finger. Right after needle puncture with attached syringe and local anaesthetic solution is conducted at a point that is 1 cm inferior to and 1 cm medial to the pubic tubercle, pass the needle directly downward in a vertical fashion, which leads it into the spermatic cord. After a check-up (negative aspiration) for bleeding, approximately 3 mL of solution (Lidocaine 2%) is injected into the cord.

    Also known as: Local aesthesia by needle injection

05

What researchers measure

Primary outcomes

  1. Pain score

    Right after completing the injection, information about the pain before, during and after the sperm retrieval technique will be immediately documented by the visual analog scale (VAS) questionnaire on 10 cm lines (0 represents no pain, whereas 10 marks the highest score).

    Time frame: 1 year

Secondary outcomes

  1. Pressure (fear) of the patients

    Right after completing the injection, information about the pain before, during and after the sperm retrieval technique will be immediately documented by the visual analog scale (VAS) questionnaire on 10 cm lines (0 represents no pain, whereas 10 marks the highest score).

    Time frame: 1 year

  2. Discomfort of the patients

    Right after completing the injection, information about the pain before, during and after the sperm retrieval technique will be immediately documented by the visual analog scale (VAS) questionnaire on 10 cm lines (0 represents no pain, whereas 10 marks the highest score).

    Time frame: 1 year

  3. Incidence of treatment (Bleeding)

    Bleeding will be recorded peri- and post- operative anesthesia.

    Time frame: 1 year

  4. Incidence of treatment (Swelling)

    Swelling will be recorded peri- and post- operative anesthesia.

    Time frame: 1 year

  5. Incidence of treatment (Hematoma)

    Hematoma will be recorded peri- and post- operative anesthesia.

    Time frame: 1 year

  6. Onset of action of Madajet

    By using the stopwatch, the onset of action of anesthesia will be recorded. Every five seconds, the pain reaction which shows the onset is determined on the scrotum by using tissue forceps.

    Time frame: 1 year

  7. Duration of action of Madajet

    By using the stopwatch, the duration of action of anesthesia will be recorded. The patients are observed in the operation room until all the symptoms of anesthesia wore off. The total duration of anesthesia is measured from the time of onset until the patient reports normal reaction in the scrotum.

    Time frame: 1 year

  8. Onset of action of Needle injection

    By using the stopwatch, the onset of action of anesthesia will be recorded. Every thirty seconds, the pain reaction which shows the onset is determined on the scrotum by using tissue forceps.

    Time frame: 1 year

  9. Duration of action of Needle injection

    By using the stopwatch, the duration of action of anesthesia will be recorded. The patients are observed in the operation room until all the symptoms of anesthesia wore off. The total duration of anesthesia is measured from the time of onset until the patient reports normal reaction in the scrotum.

    Time frame: 1 year

06

Study locations

1 site
  • My Duc Hospital
    Ho Chi Minh City, 84, Vietnam
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03181243
Lead sponsor
Vietnam National University
Responsible party
Manh Tuong Ho (Director, Vietnam National University) — Principal investigator
First posted
Jun 8, 2017
Start date
Jul 15, 2017
Primary completion
Dec 25, 2017
Completion
Dec 25, 2017
Last update
Jan 2, 2018

Study contacts

Khoa D Le, Dr
principal investigator · Mỹ Đức Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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